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NDC properties for NDC 9 24208-818

NDC item 24208081825

NDC 924208-818
NDC 1024208-818-25
NDC Item24208081825
packaging1 BOTTLE, DISPENSING in 1 CARTON (24208-818-25) / 5 mL in 1 BOTTLE, DISPENSING
FDA SPL set id567541
LabelerBausch & Lomb Incorporated
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryNDA AUTHORIZED GENERIC
Marketing effective time low2018-02-14
Marketing statusACTIVE
NDA_AUTHORIZED_GENERICNDA020330

NDC item 43598074711

NDC 943598-747
NDC 1043598-747-11
NDC Item43598074711
packaging1 BOTTLE in 1 CARTON (43598-747-11) / 5 mL in 1 BOTTLE
ANDAANDA215733
FDA SPL set id793699
LabelerDr. Reddy's Laboratories, Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2022-05-01
Marketing statusACTIVE

NDC item 60219137703

NDC 960219-1377
NDC 1060219-1377-3
NDC Item60219137703
packaging1 BOTTLE, DROPPER in 1 CARTON (60219-1377-3) / 5 mL in 1 BOTTLE, DROPPER
ANDAANDA216343
FDA SPL set id801975
LabelerAmneal Pharmaceuticals NY LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2024-05-27
Marketing statusACTIVE

NDC item 60219205403

NDC 960219-2054
NDC 1060219-2054-3
NDC Item60219205403
packaging1 BOTTLE, DROPPER in 1 CARTON (60219-2054-3) / 2.5 mL in 1 BOTTLE, DROPPER
ANDAANDA216343
FDA SPL set id801975
LabelerAmneal Pharmaceuticals NY LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2024-05-27
Marketing statusACTIVE

NDC item 61314022405

NDC 961314-224
NDC 1061314-224-05
NDC Item61314022405
packaging5 mL in 1 BOTTLE (61314-224-05)
FDA SPL set id790292
LabelerSandoz Inc
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryNDA
Marketing effective time low1998-12-24
Marketing statusACTIVE
NDANDA020963

NDC item 61314022425

NDC 961314-224
NDC 1061314-224-25
NDC Item61314022425
packaging2.5 mL in 1 BOTTLE (61314-224-25)
FDA SPL set id790292
LabelerSandoz Inc
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryNDA
Marketing effective time low1998-12-24
Marketing statusACTIVE
NDANDA020963

NDC item 62332054505

NDC 962332-545
NDC 1062332-545-05
NDC Item62332054505
packaging1 BOTTLE in 1 CARTON (62332-545-05) / 5 mL in 1 BOTTLE
ANDAANDA212942
FDA SPL set id599393
LabelerAlembic Pharmaceuticals Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2020-11-22
Marketing statusACTIVE

NDC item 68083045701

NDC 968083-457
NDC 1068083-457-01
NDC Item68083045701
packaging1 BOTTLE in 1 CARTON (68083-457-01) / 5 mL in 1 BOTTLE
ANDAANDA214645
FDA SPL set id695465
LabelerGland Pharma Limited
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2022-06-24
Marketing statusACTIVE

NDC item 70069024101

NDC 970069-241
NDC 1070069-241-01
NDC Item70069024101
packaging1 BOTTLE in 1 CARTON (70069-241-01) / 5 mL in 1 BOTTLE
ANDAANDA210640
COLORTEXTWHITE(slightly viscous colorless solution)
ColorC48325 __
FDA SPL set id827170
LabelerSomerset Therapeutics, LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2024-10-31
Marketing statusACTIVE

NDC item 72266019901

NDC 972266-199
NDC 1072266-199-01
NDC Item72266019901
packaging1 BOTTLE in 1 CARTON (72266-199-01) / 5 mL in 1 BOTTLE
ANDAANDA214645
FDA SPL set id866357
LabelerFOSUN PHARMA USA INC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2022-06-24
Marketing statusACTIVE

NDC item 72603016201

NDC 972603-162
NDC 1072603-162-01
NDC Item72603016201
packaging1 BOTTLE in 1 CARTON (72603-162-01) / 5 mL in 1 BOTTLE
ANDAANDA215733
FDA SPL set id747523
LabelerNorthStar RxLLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2023-08-14
Marketing statusACTIVE

NDC item 82260081825

NDC 982260-818
NDC 1082260-818-25
NDC Item82260081825
packaging1 BOTTLE, DISPENSING in 1 CARTON (82260-818-25) / 5 mL in 1 BOTTLE, DISPENSING
FDA SPL set id867085
LabelerBausch & Lomb Americas Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryNDA AUTHORIZED GENERIC
Marketing effective time low2018-02-14
Marketing statusACTIVE
NDA_AUTHORIZED_GENERICNDA020330