NDC properties for "timolol 0.5 % (as timolol maleate 6.8 MG/ML) 24 HR Ophthalmic Solution" (RxCUI 1992299)

About this data

The tables show NDC propoerties for timolol 0.5 % (as timolol maleate 6.8 MG/ML) 24 HR Ophthalmic Solution with the RxCUI 1992299

This product uses publicly available data from the U.S. National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services; NLM is not responsible for the product and does not endorse or recommend this or any other product

Details for timolol 0.5 % (as timolol maleate 6.8 MG/ML) 24 HR Ophthalmic Solution (RxCUI 1992299)

ANDA	ANDA204936
ANDA	ANDA216653
MMSL_CODE	BD12430
MMSL_CODE	CD12430
MMSL_CODE	MTH_RXN_BD3330
RxCUI	1992299
SPL_SET_ID	3c20b537-88c6-4ec7-a359-e0ba67afe431
SPL_SET_ID	b686bbad-1ef7-4b94-a316-4d182a40b89a
SPL_SET_ID	bfd95433-e47a-4c5c-9bdf-77bffc13544d
SPL_SET_ID	df10af59-3b72-ca33-fd89-d9fcd0d61e9b
VUID	4037944
Prescribable Synonym	timolol 0.5 % 24HR Ophthalmic Solution
RXNAV_STR	24 HR timolol 5 MG/ML Ophthalmic Solution
RxNorm Name	24 HR timolol 5 MG/ML Ophthalmic Solution
RxNorm Synonym	timolol 0.5 % (as timolol maleate 6.8 MG/ML) 24 HR Ophthalmic Solution
RxNorm Synonym	timolol 0.5 % 24 HR Ophthalmic Solution
Related queries	Interactions (for RxCUI 1992299)

NDC Properties

NDC Item 60505100501

NDC 9	60505-1005
NDC 10	60505-1005-1
NDC Item	60505100501
Packaging	1 BOTTLE, DROPPER in 1 CARTON (60505-1005-1) / 5 mL in 1 BOTTLE, DROPPER
ANDA	ANDA204936
FDA SPL set id	788504
Labeler	Apotex Corp
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	ANDA
Marketing effective time high	2025-05-31
Marketing effective time low	2017-11-27
Marketing status	COMPLETED
Related queries	Properties for NDC 9 60505-1005

NDC Item 60505100504

NDC 9	60505-1005
NDC 10	60505-1005-4
NDC Item	60505100504
Packaging	1 BOTTLE, DROPPER in 1 CARTON (60505-1005-4) / 2.5 mL in 1 BOTTLE, DROPPER
ANDA	ANDA204936
FDA SPL set id	788504
Labeler	Apotex Corp
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	ANDA
Marketing effective time high	2025-05-31
Marketing effective time low	2017-11-27
Marketing status	COMPLETED
Related queries	Properties for NDC 9 60505-1005

NDC Item 68682004525

NDC 9	68682-045
NDC 10	68682-045-25
NDC Item	68682004525
Packaging	1 BOTTLE, DROPPER in 1 CARTON (68682-045-25) / 2.5 mL in 1 BOTTLE, DROPPER
FDA SPL set id	448355
Labeler	Oceanside Pharmaceuticals
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	NDA AUTHORIZED GENERIC
Marketing effective time low	2018-05-30
Marketing status	ACTIVE
NDA_AUTHORIZED_GENERIC	NDA021516
Related queries	Properties for NDC 9 68682-045

NDC Item 68682004550

NDC 9	68682-045
NDC 10	68682-045-50
NDC Item	68682004550
Packaging	1 BOTTLE, DROPPER in 1 CARTON (68682-045-50) / 5 mL in 1 BOTTLE, DROPPER
FDA SPL set id	448355
Labeler	Oceanside Pharmaceuticals
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	NDA AUTHORIZED GENERIC
Marketing effective time low	2018-05-30
Marketing status	ACTIVE
NDA_AUTHORIZED_GENERIC	NDA021516
Related queries	Properties for NDC 9 68682-045

NDC Item 70069051601

NDC 9	70069-516
NDC 10	70069-516-01
NDC Item	70069051601
Packaging	1 BOTTLE in 1 CARTON (70069-516-01) / 2.5 mL in 1 BOTTLE
ANDA	ANDA216653
FDA SPL set id	796359
Labeler	Somerset Therapeutics, LLC
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	ANDA
Marketing effective time low	2024-07-09
Marketing status	ACTIVE
Related queries	Properties for NDC 9 70069-516

NDC Item 70069051701

NDC 9	70069-517
NDC 10	70069-517-01
NDC Item	70069051701
Packaging	1 BOTTLE in 1 CARTON (70069-517-01) / 5 mL in 1 BOTTLE
ANDA	ANDA216653
FDA SPL set id	796359
Labeler	Somerset Therapeutics, LLC
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	ANDA
Marketing effective time low	2024-07-09
Marketing status	ACTIVE
Related queries	Properties for NDC 9 70069-517

NDC Item 82260004505

NDC 9	82260-045
NDC 10	82260-045-05
NDC Item	82260004505
Packaging	1 BOTTLE, DROPPER in 1 CARTON (82260-045-05) / 5 mL in 1 BOTTLE, DROPPER
FDA SPL set id	826867
Labeler	Bausch & Lomb Americas Inc.
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	NDA AUTHORIZED GENERIC
Marketing effective time low	2022-06-23
Marketing status	ACTIVE
NDA_AUTHORIZED_GENERIC	NDA021516
Related queries	Properties for NDC 9 82260-045

NDC Item 82260004525

NDC 9	82260-045
NDC 10	82260-045-25
NDC Item	82260004525
Packaging	1 BOTTLE, DROPPER in 1 CARTON (82260-045-25) / 2.5 mL in 1 BOTTLE, DROPPER
FDA SPL set id	826867
Labeler	Bausch & Lomb Americas Inc.
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	NDA AUTHORIZED GENERIC
Marketing effective time low	2022-06-23
Marketing status	ACTIVE
NDA_AUTHORIZED_GENERIC	NDA021516
Related queries	Properties for NDC 9 82260-045

NDC Item 60505100501

NDC 9	60505-1005
NDC 10	60505-1005-1
NDC Item	60505100501
Packaging	1 BOTTLE, DROPPER in 1 CARTON (60505-1005-1) / 5 mL in 1 BOTTLE, DROPPER
ANDA	ANDA204936
FDA SPL set id	788504
Labeler	Apotex Corp
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	ANDA
Marketing effective time high	2025-05-31
Marketing effective time low	2017-11-27
Marketing status	COMPLETED
Related queries	Properties for NDC 9 60505-1005

NDC Item 60505100504

NDC 9	60505-1005
NDC 10	60505-1005-4
NDC Item	60505100504
Packaging	1 BOTTLE, DROPPER in 1 CARTON (60505-1005-4) / 2.5 mL in 1 BOTTLE, DROPPER
ANDA	ANDA204936
FDA SPL set id	788504
Labeler	Apotex Corp
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	ANDA
Marketing effective time high	2025-05-31
Marketing effective time low	2017-11-27
Marketing status	COMPLETED
Related queries	Properties for NDC 9 60505-1005

NDC Item 68682004525

NDC 9	68682-045
NDC 10	68682-045-25
NDC Item	68682004525
Packaging	1 BOTTLE, DROPPER in 1 CARTON (68682-045-25) / 2.5 mL in 1 BOTTLE, DROPPER
FDA SPL set id	448355
Labeler	Oceanside Pharmaceuticals
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	NDA AUTHORIZED GENERIC
Marketing effective time low	2018-05-30
Marketing status	ACTIVE
NDA_AUTHORIZED_GENERIC	NDA021516
Related queries	Properties for NDC 9 68682-045

NDC Item 68682004550

NDC 9	68682-045
NDC 10	68682-045-50
NDC Item	68682004550
Packaging	1 BOTTLE, DROPPER in 1 CARTON (68682-045-50) / 5 mL in 1 BOTTLE, DROPPER
FDA SPL set id	448355
Labeler	Oceanside Pharmaceuticals
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	NDA AUTHORIZED GENERIC
Marketing effective time low	2018-05-30
Marketing status	ACTIVE
NDA_AUTHORIZED_GENERIC	NDA021516
Related queries	Properties for NDC 9 68682-045

NDC Item 70069051601

NDC 9	70069-516
NDC 10	70069-516-01
NDC Item	70069051601
Packaging	1 BOTTLE in 1 CARTON (70069-516-01) / 2.5 mL in 1 BOTTLE
ANDA	ANDA216653
FDA SPL set id	796359
Labeler	Somerset Therapeutics, LLC
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	ANDA
Marketing effective time low	2024-07-09
Marketing status	ACTIVE
Related queries	Properties for NDC 9 70069-516

NDC Item 70069051701

NDC 9	70069-517
NDC 10	70069-517-01
NDC Item	70069051701
Packaging	1 BOTTLE in 1 CARTON (70069-517-01) / 5 mL in 1 BOTTLE
ANDA	ANDA216653
FDA SPL set id	796359
Labeler	Somerset Therapeutics, LLC
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	ANDA
Marketing effective time low	2024-07-09
Marketing status	ACTIVE
Related queries	Properties for NDC 9 70069-517

NDC Item 82260004505

NDC 9	82260-045
NDC 10	82260-045-05
NDC Item	82260004505
Packaging	1 BOTTLE, DROPPER in 1 CARTON (82260-045-05) / 5 mL in 1 BOTTLE, DROPPER
FDA SPL set id	826867
Labeler	Bausch & Lomb Americas Inc.
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	NDA AUTHORIZED GENERIC
Marketing effective time low	2022-06-23
Marketing status	ACTIVE
NDA_AUTHORIZED_GENERIC	NDA021516
Related queries	Properties for NDC 9 82260-045

NDC Item 82260004525

NDC 9	82260-045
NDC 10	82260-045-25
NDC Item	82260004525
Packaging	1 BOTTLE, DROPPER in 1 CARTON (82260-045-25) / 2.5 mL in 1 BOTTLE, DROPPER
FDA SPL set id	826867
Labeler	Bausch & Lomb Americas Inc.
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	NDA AUTHORIZED GENERIC
Marketing effective time low	2022-06-23
Marketing status	ACTIVE
NDA_AUTHORIZED_GENERIC	NDA021516
Related queries	Properties for NDC 9 82260-045

NDC Item 60505100501

NDC 9	60505-1005
NDC 10	60505-1005-1
NDC Item	60505100501
Packaging	1 BOTTLE, DROPPER in 1 CARTON (60505-1005-1) / 5 mL in 1 BOTTLE, DROPPER
ANDA	ANDA204936
FDA SPL set id	788504
Labeler	Apotex Corp
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	ANDA
Marketing effective time high	2025-05-31
Marketing effective time low	2017-11-27
Marketing status	COMPLETED
Related queries	Properties for NDC 9 60505-1005

NDC Item 60505100504

NDC 9	60505-1005
NDC 10	60505-1005-4
NDC Item	60505100504
Packaging	1 BOTTLE, DROPPER in 1 CARTON (60505-1005-4) / 2.5 mL in 1 BOTTLE, DROPPER
ANDA	ANDA204936
FDA SPL set id	788504
Labeler	Apotex Corp
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	ANDA
Marketing effective time high	2025-05-31
Marketing effective time low	2017-11-27
Marketing status	COMPLETED
Related queries	Properties for NDC 9 60505-1005

NDC Item 68682004525

NDC 9	68682-045
NDC 10	68682-045-25
NDC Item	68682004525
Packaging	1 BOTTLE, DROPPER in 1 CARTON (68682-045-25) / 2.5 mL in 1 BOTTLE, DROPPER
FDA SPL set id	448355
Labeler	Oceanside Pharmaceuticals
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	NDA AUTHORIZED GENERIC
Marketing effective time low	2018-05-30
Marketing status	ACTIVE
NDA_AUTHORIZED_GENERIC	NDA021516
Related queries	Properties for NDC 9 68682-045

NDC Item 68682004550

NDC 9	68682-045
NDC 10	68682-045-50
NDC Item	68682004550
Packaging	1 BOTTLE, DROPPER in 1 CARTON (68682-045-50) / 5 mL in 1 BOTTLE, DROPPER
FDA SPL set id	448355
Labeler	Oceanside Pharmaceuticals
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	NDA AUTHORIZED GENERIC
Marketing effective time low	2018-05-30
Marketing status	ACTIVE
NDA_AUTHORIZED_GENERIC	NDA021516
Related queries	Properties for NDC 9 68682-045

NDC Item 70069051601

NDC 9	70069-516
NDC 10	70069-516-01
NDC Item	70069051601
Packaging	1 BOTTLE in 1 CARTON (70069-516-01) / 2.5 mL in 1 BOTTLE
ANDA	ANDA216653
FDA SPL set id	796359
Labeler	Somerset Therapeutics, LLC
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	ANDA
Marketing effective time low	2024-07-09
Marketing status	ACTIVE
Related queries	Properties for NDC 9 70069-516

NDC Item 70069051701

NDC 9	70069-517
NDC 10	70069-517-01
NDC Item	70069051701
Packaging	1 BOTTLE in 1 CARTON (70069-517-01) / 5 mL in 1 BOTTLE
ANDA	ANDA216653
FDA SPL set id	796359
Labeler	Somerset Therapeutics, LLC
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	ANDA
Marketing effective time low	2024-07-09
Marketing status	ACTIVE
Related queries	Properties for NDC 9 70069-517

NDC Item 82260004505

NDC 9	82260-045
NDC 10	82260-045-05
NDC Item	82260004505
Packaging	1 BOTTLE, DROPPER in 1 CARTON (82260-045-05) / 5 mL in 1 BOTTLE, DROPPER
FDA SPL set id	826867
Labeler	Bausch & Lomb Americas Inc.
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	NDA AUTHORIZED GENERIC
Marketing effective time low	2022-06-23
Marketing status	ACTIVE
NDA_AUTHORIZED_GENERIC	NDA021516
Related queries	Properties for NDC 9 82260-045

NDC Item 82260004525

NDC 9	82260-045
NDC 10	82260-045-25
NDC Item	82260004525
Packaging	1 BOTTLE, DROPPER in 1 CARTON (82260-045-25) / 2.5 mL in 1 BOTTLE, DROPPER
FDA SPL set id	826867
Labeler	Bausch & Lomb Americas Inc.
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	NDA AUTHORIZED GENERIC
Marketing effective time low	2022-06-23
Marketing status	ACTIVE
NDA_AUTHORIZED_GENERIC	NDA021516
Related queries	Properties for NDC 9 82260-045

NDC Item 60505100501

NDC 9	60505-1005
NDC 10	60505-1005-1
NDC Item	60505100501
Packaging	1 BOTTLE, DROPPER in 1 CARTON (60505-1005-1) / 5 mL in 1 BOTTLE, DROPPER
ANDA	ANDA204936
FDA SPL set id	788504
Labeler	Apotex Corp
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	ANDA
Marketing effective time high	2025-05-31
Marketing effective time low	2017-11-27
Marketing status	COMPLETED
Related queries	Properties for NDC 9 60505-1005

NDC Item 60505100504

NDC 9	60505-1005
NDC 10	60505-1005-4
NDC Item	60505100504
Packaging	1 BOTTLE, DROPPER in 1 CARTON (60505-1005-4) / 2.5 mL in 1 BOTTLE, DROPPER
ANDA	ANDA204936
FDA SPL set id	788504
Labeler	Apotex Corp
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	ANDA
Marketing effective time high	2025-05-31
Marketing effective time low	2017-11-27
Marketing status	COMPLETED
Related queries	Properties for NDC 9 60505-1005

NDC Item 68682004525

NDC 9	68682-045
NDC 10	68682-045-25
NDC Item	68682004525
Packaging	1 BOTTLE, DROPPER in 1 CARTON (68682-045-25) / 2.5 mL in 1 BOTTLE, DROPPER
FDA SPL set id	448355
Labeler	Oceanside Pharmaceuticals
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	NDA AUTHORIZED GENERIC
Marketing effective time low	2018-05-30
Marketing status	ACTIVE
NDA_AUTHORIZED_GENERIC	NDA021516
Related queries	Properties for NDC 9 68682-045

NDC Item 68682004550

NDC 9	68682-045
NDC 10	68682-045-50
NDC Item	68682004550
Packaging	1 BOTTLE, DROPPER in 1 CARTON (68682-045-50) / 5 mL in 1 BOTTLE, DROPPER
FDA SPL set id	448355
Labeler	Oceanside Pharmaceuticals
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	NDA AUTHORIZED GENERIC
Marketing effective time low	2018-05-30
Marketing status	ACTIVE
NDA_AUTHORIZED_GENERIC	NDA021516
Related queries	Properties for NDC 9 68682-045

NDC Item 70069051601

NDC 9	70069-516
NDC 10	70069-516-01
NDC Item	70069051601
Packaging	1 BOTTLE in 1 CARTON (70069-516-01) / 2.5 mL in 1 BOTTLE
ANDA	ANDA216653
FDA SPL set id	796359
Labeler	Somerset Therapeutics, LLC
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	ANDA
Marketing effective time low	2024-07-09
Marketing status	ACTIVE
Related queries	Properties for NDC 9 70069-516

NDC Item 70069051701

NDC 9	70069-517
NDC 10	70069-517-01
NDC Item	70069051701
Packaging	1 BOTTLE in 1 CARTON (70069-517-01) / 5 mL in 1 BOTTLE
ANDA	ANDA216653
FDA SPL set id	796359
Labeler	Somerset Therapeutics, LLC
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	ANDA
Marketing effective time low	2024-07-09
Marketing status	ACTIVE
Related queries	Properties for NDC 9 70069-517

NDC Item 82260004505

NDC 9	82260-045
NDC 10	82260-045-05
NDC Item	82260004505
Packaging	1 BOTTLE, DROPPER in 1 CARTON (82260-045-05) / 5 mL in 1 BOTTLE, DROPPER
FDA SPL set id	826867
Labeler	Bausch & Lomb Americas Inc.
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	NDA AUTHORIZED GENERIC
Marketing effective time low	2022-06-23
Marketing status	ACTIVE
NDA_AUTHORIZED_GENERIC	NDA021516
Related queries	Properties for NDC 9 82260-045

NDC Item 82260004525

NDC 9	82260-045
NDC 10	82260-045-25
NDC Item	82260004525
Packaging	1 BOTTLE, DROPPER in 1 CARTON (82260-045-25) / 2.5 mL in 1 BOTTLE, DROPPER
FDA SPL set id	826867
Labeler	Bausch & Lomb Americas Inc.
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	NDA AUTHORIZED GENERIC
Marketing effective time low	2022-06-23
Marketing status	ACTIVE
NDA_AUTHORIZED_GENERIC	NDA021516
Related queries	Properties for NDC 9 82260-045

NDC Item 60505100501

NDC 9	60505-1005
NDC 10	60505-1005-1
NDC Item	60505100501
Packaging	1 BOTTLE, DROPPER in 1 CARTON (60505-1005-1) / 5 mL in 1 BOTTLE, DROPPER
ANDA	ANDA204936
FDA SPL set id	788504
Labeler	Apotex Corp
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	ANDA
Marketing effective time high	2025-05-31
Marketing effective time low	2017-11-27
Marketing status	COMPLETED
Related queries	Properties for NDC 9 60505-1005

NDC Item 60505100504

NDC 9	60505-1005
NDC 10	60505-1005-4
NDC Item	60505100504
Packaging	1 BOTTLE, DROPPER in 1 CARTON (60505-1005-4) / 2.5 mL in 1 BOTTLE, DROPPER
ANDA	ANDA204936
FDA SPL set id	788504
Labeler	Apotex Corp
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	ANDA
Marketing effective time high	2025-05-31
Marketing effective time low	2017-11-27
Marketing status	COMPLETED
Related queries	Properties for NDC 9 60505-1005

NDC Item 68682004525

NDC 9	68682-045
NDC 10	68682-045-25
NDC Item	68682004525
Packaging	1 BOTTLE, DROPPER in 1 CARTON (68682-045-25) / 2.5 mL in 1 BOTTLE, DROPPER
FDA SPL set id	448355
Labeler	Oceanside Pharmaceuticals
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	NDA AUTHORIZED GENERIC
Marketing effective time low	2018-05-30
Marketing status	ACTIVE
NDA_AUTHORIZED_GENERIC	NDA021516
Related queries	Properties for NDC 9 68682-045

NDC Item 68682004550

NDC 9	68682-045
NDC 10	68682-045-50
NDC Item	68682004550
Packaging	1 BOTTLE, DROPPER in 1 CARTON (68682-045-50) / 5 mL in 1 BOTTLE, DROPPER
FDA SPL set id	448355
Labeler	Oceanside Pharmaceuticals
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	NDA AUTHORIZED GENERIC
Marketing effective time low	2018-05-30
Marketing status	ACTIVE
NDA_AUTHORIZED_GENERIC	NDA021516
Related queries	Properties for NDC 9 68682-045

NDC Item 70069051601

NDC 9	70069-516
NDC 10	70069-516-01
NDC Item	70069051601
Packaging	1 BOTTLE in 1 CARTON (70069-516-01) / 2.5 mL in 1 BOTTLE
ANDA	ANDA216653
FDA SPL set id	796359
Labeler	Somerset Therapeutics, LLC
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	ANDA
Marketing effective time low	2024-07-09
Marketing status	ACTIVE
Related queries	Properties for NDC 9 70069-516

NDC Item 70069051701

NDC 9	70069-517
NDC 10	70069-517-01
NDC Item	70069051701
Packaging	1 BOTTLE in 1 CARTON (70069-517-01) / 5 mL in 1 BOTTLE
ANDA	ANDA216653
FDA SPL set id	796359
Labeler	Somerset Therapeutics, LLC
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	ANDA
Marketing effective time low	2024-07-09
Marketing status	ACTIVE
Related queries	Properties for NDC 9 70069-517

NDC Item 82260004505

NDC 9	82260-045
NDC 10	82260-045-05
NDC Item	82260004505
Packaging	1 BOTTLE, DROPPER in 1 CARTON (82260-045-05) / 5 mL in 1 BOTTLE, DROPPER
FDA SPL set id	826867
Labeler	Bausch & Lomb Americas Inc.
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	NDA AUTHORIZED GENERIC
Marketing effective time low	2022-06-23
Marketing status	ACTIVE
NDA_AUTHORIZED_GENERIC	NDA021516
Related queries	Properties for NDC 9 82260-045

NDC Item 82260004525

NDC 9	82260-045
NDC 10	82260-045-25
NDC Item	82260004525
Packaging	1 BOTTLE, DROPPER in 1 CARTON (82260-045-25) / 2.5 mL in 1 BOTTLE, DROPPER
FDA SPL set id	826867
Labeler	Bausch & Lomb Americas Inc.
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	NDA AUTHORIZED GENERIC
Marketing effective time low	2022-06-23
Marketing status	ACTIVE
NDA_AUTHORIZED_GENERIC	NDA021516
Related queries	Properties for NDC 9 82260-045

NDC Item 60505100501

NDC 9	60505-1005
NDC 10	60505-1005-1
NDC Item	60505100501
Packaging	1 BOTTLE, DROPPER in 1 CARTON (60505-1005-1) / 5 mL in 1 BOTTLE, DROPPER
ANDA	ANDA204936
FDA SPL set id	788504
Labeler	Apotex Corp
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	ANDA
Marketing effective time high	2025-05-31
Marketing effective time low	2017-11-27
Marketing status	COMPLETED
Related queries	Properties for NDC 9 60505-1005

NDC Item 60505100504

NDC 9	60505-1005
NDC 10	60505-1005-4
NDC Item	60505100504
Packaging	1 BOTTLE, DROPPER in 1 CARTON (60505-1005-4) / 2.5 mL in 1 BOTTLE, DROPPER
ANDA	ANDA204936
FDA SPL set id	788504
Labeler	Apotex Corp
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	ANDA
Marketing effective time high	2025-05-31
Marketing effective time low	2017-11-27
Marketing status	COMPLETED
Related queries	Properties for NDC 9 60505-1005

NDC Item 68682004525

NDC 9	68682-045
NDC 10	68682-045-25
NDC Item	68682004525
Packaging	1 BOTTLE, DROPPER in 1 CARTON (68682-045-25) / 2.5 mL in 1 BOTTLE, DROPPER
FDA SPL set id	448355
Labeler	Oceanside Pharmaceuticals
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	NDA AUTHORIZED GENERIC
Marketing effective time low	2018-05-30
Marketing status	ACTIVE
NDA_AUTHORIZED_GENERIC	NDA021516
Related queries	Properties for NDC 9 68682-045

NDC Item 68682004550

NDC 9	68682-045
NDC 10	68682-045-50
NDC Item	68682004550
Packaging	1 BOTTLE, DROPPER in 1 CARTON (68682-045-50) / 5 mL in 1 BOTTLE, DROPPER
FDA SPL set id	448355
Labeler	Oceanside Pharmaceuticals
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	NDA AUTHORIZED GENERIC
Marketing effective time low	2018-05-30
Marketing status	ACTIVE
NDA_AUTHORIZED_GENERIC	NDA021516
Related queries	Properties for NDC 9 68682-045

NDC Item 70069051601

NDC 9	70069-516
NDC 10	70069-516-01
NDC Item	70069051601
Packaging	1 BOTTLE in 1 CARTON (70069-516-01) / 2.5 mL in 1 BOTTLE
ANDA	ANDA216653
FDA SPL set id	796359
Labeler	Somerset Therapeutics, LLC
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	ANDA
Marketing effective time low	2024-07-09
Marketing status	ACTIVE
Related queries	Properties for NDC 9 70069-516

NDC Item 70069051701

NDC 9	70069-517
NDC 10	70069-517-01
NDC Item	70069051701
Packaging	1 BOTTLE in 1 CARTON (70069-517-01) / 5 mL in 1 BOTTLE
ANDA	ANDA216653
FDA SPL set id	796359
Labeler	Somerset Therapeutics, LLC
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	ANDA
Marketing effective time low	2024-07-09
Marketing status	ACTIVE
Related queries	Properties for NDC 9 70069-517

NDC Item 82260004505

NDC 9	82260-045
NDC 10	82260-045-05
NDC Item	82260004505
Packaging	1 BOTTLE, DROPPER in 1 CARTON (82260-045-05) / 5 mL in 1 BOTTLE, DROPPER
FDA SPL set id	826867
Labeler	Bausch & Lomb Americas Inc.
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	NDA AUTHORIZED GENERIC
Marketing effective time low	2022-06-23
Marketing status	ACTIVE
NDA_AUTHORIZED_GENERIC	NDA021516
Related queries	Properties for NDC 9 82260-045

NDC Item 82260004525

NDC 9	82260-045
NDC 10	82260-045-25
NDC Item	82260004525
Packaging	1 BOTTLE, DROPPER in 1 CARTON (82260-045-25) / 2.5 mL in 1 BOTTLE, DROPPER
FDA SPL set id	826867
Labeler	Bausch & Lomb Americas Inc.
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	NDA AUTHORIZED GENERIC
Marketing effective time low	2022-06-23
Marketing status	ACTIVE
NDA_AUTHORIZED_GENERIC	NDA021516
Related queries	Properties for NDC 9 82260-045

NDC Item 60505100501

NDC 9	60505-1005
NDC 10	60505-1005-1
NDC Item	60505100501
Packaging	1 BOTTLE, DROPPER in 1 CARTON (60505-1005-1) / 5 mL in 1 BOTTLE, DROPPER
ANDA	ANDA204936
FDA SPL set id	788504
Labeler	Apotex Corp
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	ANDA
Marketing effective time high	2025-05-31
Marketing effective time low	2017-11-27
Marketing status	COMPLETED
Related queries	Properties for NDC 9 60505-1005

NDC Item 60505100504

NDC 9	60505-1005
NDC 10	60505-1005-4
NDC Item	60505100504
Packaging	1 BOTTLE, DROPPER in 1 CARTON (60505-1005-4) / 2.5 mL in 1 BOTTLE, DROPPER
ANDA	ANDA204936
FDA SPL set id	788504
Labeler	Apotex Corp
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	ANDA
Marketing effective time high	2025-05-31
Marketing effective time low	2017-11-27
Marketing status	COMPLETED
Related queries	Properties for NDC 9 60505-1005

NDC Item 68682004525

NDC 9	68682-045
NDC 10	68682-045-25
NDC Item	68682004525
Packaging	1 BOTTLE, DROPPER in 1 CARTON (68682-045-25) / 2.5 mL in 1 BOTTLE, DROPPER
FDA SPL set id	448355
Labeler	Oceanside Pharmaceuticals
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	NDA AUTHORIZED GENERIC
Marketing effective time low	2018-05-30
Marketing status	ACTIVE
NDA_AUTHORIZED_GENERIC	NDA021516
Related queries	Properties for NDC 9 68682-045

NDC Item 68682004550

NDC 9	68682-045
NDC 10	68682-045-50
NDC Item	68682004550
Packaging	1 BOTTLE, DROPPER in 1 CARTON (68682-045-50) / 5 mL in 1 BOTTLE, DROPPER
FDA SPL set id	448355
Labeler	Oceanside Pharmaceuticals
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	NDA AUTHORIZED GENERIC
Marketing effective time low	2018-05-30
Marketing status	ACTIVE
NDA_AUTHORIZED_GENERIC	NDA021516
Related queries	Properties for NDC 9 68682-045

NDC Item 70069051601

NDC 9	70069-516
NDC 10	70069-516-01
NDC Item	70069051601
Packaging	1 BOTTLE in 1 CARTON (70069-516-01) / 2.5 mL in 1 BOTTLE
ANDA	ANDA216653
FDA SPL set id	796359
Labeler	Somerset Therapeutics, LLC
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	ANDA
Marketing effective time low	2024-07-09
Marketing status	ACTIVE
Related queries	Properties for NDC 9 70069-516

NDC Item 70069051701

NDC 9	70069-517
NDC 10	70069-517-01
NDC Item	70069051701
Packaging	1 BOTTLE in 1 CARTON (70069-517-01) / 5 mL in 1 BOTTLE
ANDA	ANDA216653
FDA SPL set id	796359
Labeler	Somerset Therapeutics, LLC
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	ANDA
Marketing effective time low	2024-07-09
Marketing status	ACTIVE
Related queries	Properties for NDC 9 70069-517

NDC Item 82260004505

NDC 9	82260-045
NDC 10	82260-045-05
NDC Item	82260004505
Packaging	1 BOTTLE, DROPPER in 1 CARTON (82260-045-05) / 5 mL in 1 BOTTLE, DROPPER
FDA SPL set id	826867
Labeler	Bausch & Lomb Americas Inc.
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	NDA AUTHORIZED GENERIC
Marketing effective time low	2022-06-23
Marketing status	ACTIVE
NDA_AUTHORIZED_GENERIC	NDA021516
Related queries	Properties for NDC 9 82260-045

NDC Item 82260004525

NDC 9	82260-045
NDC 10	82260-045-25
NDC Item	82260004525
Packaging	1 BOTTLE, DROPPER in 1 CARTON (82260-045-25) / 2.5 mL in 1 BOTTLE, DROPPER
FDA SPL set id	826867
Labeler	Bausch & Lomb Americas Inc.
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	NDA AUTHORIZED GENERIC
Marketing effective time low	2022-06-23
Marketing status	ACTIVE
NDA_AUTHORIZED_GENERIC	NDA021516
Related queries	Properties for NDC 9 82260-045

NDC Item 60505100501

NDC 9	60505-1005
NDC 10	60505-1005-1
NDC Item	60505100501
Packaging	1 BOTTLE, DROPPER in 1 CARTON (60505-1005-1) / 5 mL in 1 BOTTLE, DROPPER
ANDA	ANDA204936
FDA SPL set id	788504
Labeler	Apotex Corp
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	ANDA
Marketing effective time high	2025-05-31
Marketing effective time low	2017-11-27
Marketing status	COMPLETED
Related queries	Properties for NDC 9 60505-1005

NDC Item 60505100504

NDC 9	60505-1005
NDC 10	60505-1005-4
NDC Item	60505100504
Packaging	1 BOTTLE, DROPPER in 1 CARTON (60505-1005-4) / 2.5 mL in 1 BOTTLE, DROPPER
ANDA	ANDA204936
FDA SPL set id	788504
Labeler	Apotex Corp
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	ANDA
Marketing effective time high	2025-05-31
Marketing effective time low	2017-11-27
Marketing status	COMPLETED
Related queries	Properties for NDC 9 60505-1005

NDC Item 68682004525

NDC 9	68682-045
NDC 10	68682-045-25
NDC Item	68682004525
Packaging	1 BOTTLE, DROPPER in 1 CARTON (68682-045-25) / 2.5 mL in 1 BOTTLE, DROPPER
FDA SPL set id	448355
Labeler	Oceanside Pharmaceuticals
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	NDA AUTHORIZED GENERIC
Marketing effective time low	2018-05-30
Marketing status	ACTIVE
NDA_AUTHORIZED_GENERIC	NDA021516
Related queries	Properties for NDC 9 68682-045

NDC Item 68682004550

NDC 9	68682-045
NDC 10	68682-045-50
NDC Item	68682004550
Packaging	1 BOTTLE, DROPPER in 1 CARTON (68682-045-50) / 5 mL in 1 BOTTLE, DROPPER
FDA SPL set id	448355
Labeler	Oceanside Pharmaceuticals
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	NDA AUTHORIZED GENERIC
Marketing effective time low	2018-05-30
Marketing status	ACTIVE
NDA_AUTHORIZED_GENERIC	NDA021516
Related queries	Properties for NDC 9 68682-045

NDC Item 70069051601

NDC 9	70069-516
NDC 10	70069-516-01
NDC Item	70069051601
Packaging	1 BOTTLE in 1 CARTON (70069-516-01) / 2.5 mL in 1 BOTTLE
ANDA	ANDA216653
FDA SPL set id	796359
Labeler	Somerset Therapeutics, LLC
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	ANDA
Marketing effective time low	2024-07-09
Marketing status	ACTIVE
Related queries	Properties for NDC 9 70069-516

NDC Item 70069051701

NDC 9	70069-517
NDC 10	70069-517-01
NDC Item	70069051701
Packaging	1 BOTTLE in 1 CARTON (70069-517-01) / 5 mL in 1 BOTTLE
ANDA	ANDA216653
FDA SPL set id	796359
Labeler	Somerset Therapeutics, LLC
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	ANDA
Marketing effective time low	2024-07-09
Marketing status	ACTIVE
Related queries	Properties for NDC 9 70069-517

NDC Item 82260004505

NDC 9	82260-045
NDC 10	82260-045-05
NDC Item	82260004505
Packaging	1 BOTTLE, DROPPER in 1 CARTON (82260-045-05) / 5 mL in 1 BOTTLE, DROPPER
FDA SPL set id	826867
Labeler	Bausch & Lomb Americas Inc.
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	NDA AUTHORIZED GENERIC
Marketing effective time low	2022-06-23
Marketing status	ACTIVE
NDA_AUTHORIZED_GENERIC	NDA021516
Related queries	Properties for NDC 9 82260-045

NDC Item 82260004525

NDC 9	82260-045
NDC 10	82260-045-25
NDC Item	82260004525
Packaging	1 BOTTLE, DROPPER in 1 CARTON (82260-045-25) / 2.5 mL in 1 BOTTLE, DROPPER
FDA SPL set id	826867
Labeler	Bausch & Lomb Americas Inc.
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	NDA AUTHORIZED GENERIC
Marketing effective time low	2022-06-23
Marketing status	ACTIVE
NDA_AUTHORIZED_GENERIC	NDA021516
Related queries	Properties for NDC 9 82260-045