NDC properties for "eribulin mesylate 1 MG per 2 ML Injection" (RxCUI 1045456)

About this data

The tables show NDC propoerties for eribulin mesylate 1 MG per 2 ML Injection with the RxCUI 1045456

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 eribulin mesylate 1 MG per 2 ML Injection (RxCUI 1045456)

ANDA	ANDA214850
ANDA	ANDA218047
ANDA	ANDA218281
MMSL_CODE	BD26641
MMSL_CODE	CD26641
RxCUI	1045456
SPL_SET_ID	4a64918a-f674-4843-b544-ab815fdd1b8f
SPL_SET_ID	7752b084-cdc7-6eac-e294-e45db82c372a
SPL_SET_ID	aa69e7a5-fa82-4984-b9d2-653c772b80e3
SPL_SET_ID	f57835e2-4c53-4e93-b54b-7d7a5000ae3d
VUID	4030274
Prescribable Synonym	eriBULin mesylate 1 MG in 2 ML Injection
RXNAV_STR	2 ML eriBULin mesylate 0.5 MG/ML Injection
RxNorm Name	2 ML eribulin mesylate 0.5 MG/ML Injection
RxNorm Synonym	eribulin mesylate 1 MG per 2 ML Injection
Tallman Synonym	2 ML eriBULin mesylate 0.5 MG/ML Injection
Tallman Synonym	eriBULin mesylate 1 MG per 2 ML Injection
Related queries	Interactions (for RxCUI 1045456)

NDC Properties

NDC Item 00143916701

NDC 9	0143-9167
NDC 10	0143-9167-01
NDC Item	00143916701
Packaging	1 VIAL, SINGLE-DOSE in 1 CARTON (0143-9167-01) / 2 mL in 1 VIAL, SINGLE-DOSE
ANDA	ANDA218281
FDA SPL set id	796857
Labeler	HIKMA PHARMACEUTICALS USA INC.
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	ANDA
Marketing effective time low	2024-06-28
Marketing status	active
Related queries	Properties for NDC 9 0143-9167

NDC Item 60505628900

NDC 9	60505-6289
NDC 10	60505-6289-0
NDC Item	60505628900
Packaging	1 VIAL, SINGLE-DOSE in 1 CARTON (60505-6289-0) / 2 mL in 1 VIAL, SINGLE-DOSE
ANDA	ANDA218047
FDA SPL set id	785024
Labeler	Apotex Corp.
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	ANDA
Marketing effective time low	2024-05-06
Marketing status	ACTIVE
Related queries	Properties for NDC 9 60505-6289

NDC Item 68083059201

NDC 9	68083-592
NDC 10	68083-592-01
NDC Item	68083059201
Packaging	1 VIAL, SINGLE-DOSE in 1 CARTON (68083-592-01) / 2 mL in 1 VIAL, SINGLE-DOSE
ANDA	ANDA218047
FDA SPL set id	780904
Labeler	Gland Pharma Limited
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	ANDA
Marketing effective time low	2024-04-05
Marketing status	ACTIVE
Related queries	Properties for NDC 9 68083-592

NDC Item 81298389001

NDC 9	81298-3890
NDC 10	81298-3890-1
NDC Item	81298389001
Packaging	1 VIAL, SINGLE-DOSE in 1 CARTON (81298-3890-1) / 2 mL in 1 VIAL, SINGLE-DOSE
ANDA	ANDA214850
FDA SPL set id	800808
Labeler	Long Grove Pharmaceuticals, LLC
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	ANDA
Marketing effective time low	2024-07-22
Marketing status	active
Related queries	Properties for NDC 9 81298-3890

NDC Item 00143916701

NDC 9	0143-9167
NDC 10	0143-9167-01
NDC Item	00143916701
Packaging	1 VIAL, SINGLE-DOSE in 1 CARTON (0143-9167-01) / 2 mL in 1 VIAL, SINGLE-DOSE
ANDA	ANDA218281
FDA SPL set id	796857
Labeler	HIKMA PHARMACEUTICALS USA INC.
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	ANDA
Marketing effective time low	2024-06-28
Marketing status	active
Related queries	Properties for NDC 9 0143-9167

NDC Item 60505628900

NDC 9	60505-6289
NDC 10	60505-6289-0
NDC Item	60505628900
Packaging	1 VIAL, SINGLE-DOSE in 1 CARTON (60505-6289-0) / 2 mL in 1 VIAL, SINGLE-DOSE
ANDA	ANDA218047
FDA SPL set id	785024
Labeler	Apotex Corp.
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	ANDA
Marketing effective time low	2024-05-06
Marketing status	ACTIVE
Related queries	Properties for NDC 9 60505-6289

NDC Item 68083059201

NDC 9	68083-592
NDC 10	68083-592-01
NDC Item	68083059201
Packaging	1 VIAL, SINGLE-DOSE in 1 CARTON (68083-592-01) / 2 mL in 1 VIAL, SINGLE-DOSE
ANDA	ANDA218047
FDA SPL set id	780904
Labeler	Gland Pharma Limited
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	ANDA
Marketing effective time low	2024-04-05
Marketing status	ACTIVE
Related queries	Properties for NDC 9 68083-592

NDC Item 81298389001

NDC 9	81298-3890
NDC 10	81298-3890-1
NDC Item	81298389001
Packaging	1 VIAL, SINGLE-DOSE in 1 CARTON (81298-3890-1) / 2 mL in 1 VIAL, SINGLE-DOSE
ANDA	ANDA214850
FDA SPL set id	800808
Labeler	Long Grove Pharmaceuticals, LLC
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	ANDA
Marketing effective time low	2024-07-22
Marketing status	active
Related queries	Properties for NDC 9 81298-3890

NDC Item 00143916701

NDC 9	0143-9167
NDC 10	0143-9167-01
NDC Item	00143916701
Packaging	1 VIAL, SINGLE-DOSE in 1 CARTON (0143-9167-01) / 2 mL in 1 VIAL, SINGLE-DOSE
ANDA	ANDA218281
FDA SPL set id	796857
Labeler	HIKMA PHARMACEUTICALS USA INC.
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	ANDA
Marketing effective time low	2024-06-28
Marketing status	active
Related queries	Properties for NDC 9 0143-9167

NDC Item 60505628900

NDC 9	60505-6289
NDC 10	60505-6289-0
NDC Item	60505628900
Packaging	1 VIAL, SINGLE-DOSE in 1 CARTON (60505-6289-0) / 2 mL in 1 VIAL, SINGLE-DOSE
ANDA	ANDA218047
FDA SPL set id	785024
Labeler	Apotex Corp.
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	ANDA
Marketing effective time low	2024-05-06
Marketing status	ACTIVE
Related queries	Properties for NDC 9 60505-6289

NDC Item 68083059201

NDC 9	68083-592
NDC 10	68083-592-01
NDC Item	68083059201
Packaging	1 VIAL, SINGLE-DOSE in 1 CARTON (68083-592-01) / 2 mL in 1 VIAL, SINGLE-DOSE
ANDA	ANDA218047
FDA SPL set id	780904
Labeler	Gland Pharma Limited
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	ANDA
Marketing effective time low	2024-04-05
Marketing status	ACTIVE
Related queries	Properties for NDC 9 68083-592

NDC Item 81298389001

NDC 9	81298-3890
NDC 10	81298-3890-1
NDC Item	81298389001
Packaging	1 VIAL, SINGLE-DOSE in 1 CARTON (81298-3890-1) / 2 mL in 1 VIAL, SINGLE-DOSE
ANDA	ANDA214850
FDA SPL set id	800808
Labeler	Long Grove Pharmaceuticals, LLC
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	ANDA
Marketing effective time low	2024-07-22
Marketing status	active
Related queries	Properties for NDC 9 81298-3890

NDC Item 00143916701

NDC 9	0143-9167
NDC 10	0143-9167-01
NDC Item	00143916701
Packaging	1 VIAL, SINGLE-DOSE in 1 CARTON (0143-9167-01) / 2 mL in 1 VIAL, SINGLE-DOSE
ANDA	ANDA218281
FDA SPL set id	796857
Labeler	HIKMA PHARMACEUTICALS USA INC.
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	ANDA
Marketing effective time low	2024-06-28
Marketing status	active
Related queries	Properties for NDC 9 0143-9167

NDC Item 60505628900

NDC 9	60505-6289
NDC 10	60505-6289-0
NDC Item	60505628900
Packaging	1 VIAL, SINGLE-DOSE in 1 CARTON (60505-6289-0) / 2 mL in 1 VIAL, SINGLE-DOSE
ANDA	ANDA218047
FDA SPL set id	785024
Labeler	Apotex Corp.
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	ANDA
Marketing effective time low	2024-05-06
Marketing status	ACTIVE
Related queries	Properties for NDC 9 60505-6289

NDC Item 68083059201

NDC 9	68083-592
NDC 10	68083-592-01
NDC Item	68083059201
Packaging	1 VIAL, SINGLE-DOSE in 1 CARTON (68083-592-01) / 2 mL in 1 VIAL, SINGLE-DOSE
ANDA	ANDA218047
FDA SPL set id	780904
Labeler	Gland Pharma Limited
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	ANDA
Marketing effective time low	2024-04-05
Marketing status	ACTIVE
Related queries	Properties for NDC 9 68083-592

NDC Item 81298389001

NDC 9	81298-3890
NDC 10	81298-3890-1
NDC Item	81298389001
Packaging	1 VIAL, SINGLE-DOSE in 1 CARTON (81298-3890-1) / 2 mL in 1 VIAL, SINGLE-DOSE
ANDA	ANDA214850
FDA SPL set id	800808
Labeler	Long Grove Pharmaceuticals, LLC
Label type	HUMAN PRESCRIPTION DRUG
Marketing category	ANDA
Marketing effective time low	2024-07-22
Marketing status	active
Related queries	Properties for NDC 9 81298-3890