RxSearch
HomeSearchNDC id 1923428

NDC properties for NDC 9 16571-140

NDC item 16571014010

NDC 916571-140
NDC 1016571-140-10
NDC Item16571014010
packaging1 BOTTLE in 1 CARTON (16571-140-10) / 10 mL in 1 BOTTLE
ANDAANDA077259
LabelerRising Pharma Holdings, Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing statusCOMPLETED

NDC item 16571014015

NDC 916571-140
NDC 1016571-140-15
NDC Item16571014015
packaging1 BOTTLE in 1 CARTON (16571-140-15) / 15 mL in 1 BOTTLE
ANDAANDA077259
LabelerRising Pharma Holdings, Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing statusCOMPLETED

NDC item 16571014050

NDC 916571-140
NDC 1016571-140-50
NDC Item16571014050
packaging1 BOTTLE in 1 CARTON (16571-140-50) / 5 mL in 1 BOTTLE
ANDAANDA077259
LabelerRising Pharma Holdings, Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing statusCOMPLETED

NDC item 42571040321

NDC 942571-403
NDC 1042571-403-21
NDC Item42571040321
packaging5 mL in 1 BOTTLE (42571-403-21)
ANDAANDA217343
FDA SPL set id813651
LabelerMicro Labs Limited
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2023-08-01
Marketing statusACTIVE

NDC item 42571040388

NDC 942571-403
NDC 1042571-403-88
NDC Item42571040388
packaging10 mL in 1 BOTTLE (42571-403-88)
ANDAANDA217343
FDA SPL set id813651
LabelerMicro Labs Limited
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2023-08-01
Marketing statusACTIVE

NDC item 55545100001

NDC 955545-1000
NDC 1055545-1000-1
NDC Item55545100001
packaging1 BOTTLE in 1 CARTON (55545-1000-1) / 5 mL in 1 BOTTLE
ANDAANDA077259
APPROVED_DRUG_PRODUCT_MANUFACTURED_UNDER_CONTRACTANDA077259
FDA SPL set id281715
LabelerFDC Limited
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryAPPROVED DRUG PRODUCT MANUFACTURED UNDER CONTRACT
Marketing effective time low2014-12-15
Marketing statusACTIVE

NDC item 55545100002

NDC 955545-1000
NDC 1055545-1000-2
NDC Item55545100002
packaging1 BOTTLE in 1 CARTON (55545-1000-2) / 10 mL in 1 BOTTLE
ANDAANDA077259
APPROVED_DRUG_PRODUCT_MANUFACTURED_UNDER_CONTRACTANDA077259
FDA SPL set id281715
LabelerFDC Limited
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryAPPROVED DRUG PRODUCT MANUFACTURED UNDER CONTRACT
Marketing effective time low2014-12-15
Marketing statusACTIVE

NDC item 55545100003

NDC 955545-1000
NDC 1055545-1000-3
NDC Item55545100003
packaging1 BOTTLE in 1 CARTON (55545-1000-3) / 15 mL in 1 BOTTLE
ANDAANDA077259
APPROVED_DRUG_PRODUCT_MANUFACTURED_UNDER_CONTRACTANDA077259
FDA SPL set id281715
LabelerFDC Limited
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryAPPROVED DRUG PRODUCT MANUFACTURED UNDER CONTRACT
Marketing effective time low2014-12-15
Marketing statusACTIVE

NDC item 60758080205

NDC 960758-802
NDC 1060758-802-05
NDC Item60758080205
packaging1 BOTTLE, DROPPER in 1 CARTON (60758-802-05) / 5 mL in 1 BOTTLE, DROPPER
ANDAANDA074746
COLORTEXTwhite(clear/ light yellow)
ColorC48325 __
FDA SPL set id600609
LabelerPacific Pharma, Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low1997-05-20
Marketing statusACTIVE

NDC item 60758080210

NDC 960758-802
NDC 1060758-802-10
NDC Item60758080210
packaging1 BOTTLE, DROPPER in 1 CARTON (60758-802-10) / 10 mL in 1 BOTTLE, DROPPER
ANDAANDA074746
COLORTEXTwhite(clear/ light yellow)
ColorC48325 __
FDA SPL set id600609
LabelerPacific Pharma, Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low1997-05-20
Marketing statusACTIVE

NDC item 61314022605

NDC 961314-226
NDC 1061314-226-05
NDC Item61314022605
packaging5 mL in 1 BOTTLE, PLASTIC (61314-226-05)
ANDAANDA074261
FDA SPL set id804173
LabelerSandoz Inc
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low1996-01-15
Marketing statusACTIVE

NDC item 61314022610

NDC 961314-226
NDC 1061314-226-10
NDC Item61314022610
packaging10 mL in 1 BOTTLE, PLASTIC (61314-226-10)
ANDAANDA074261
FDA SPL set id804173
LabelerSandoz Inc
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low1996-01-15
Marketing statusACTIVE

NDC item 61314022615

NDC 961314-226
NDC 1061314-226-15
NDC Item61314022615
packaging15 mL in 1 BOTTLE, PLASTIC (61314-226-15)
ANDAANDA074261
FDA SPL set id804173
LabelerSandoz Inc
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low1996-01-15
Marketing statusACTIVE

NDC item 64980051301

NDC 964980-513
NDC 1064980-513-01
NDC Item64980051301
packaging1 BOTTLE in 1 CARTON (64980-513-01) / 10 mL in 1 BOTTLE
ANDAANDA077259
FDA SPL set id804336
LabelerRising Pharma Holdings, Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2014-12-15
Marketing statusACTIVE

NDC item 64980051305

NDC 964980-513
NDC 1064980-513-05
NDC Item64980051305
packaging1 BOTTLE in 1 CARTON (64980-513-05) / 5 mL in 1 BOTTLE
ANDAANDA077259
FDA SPL set id804336
LabelerRising Pharma Holdings, Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2014-12-15
Marketing statusACTIVE

NDC item 64980051315

NDC 964980-513
NDC 1064980-513-15
NDC Item64980051315
packaging1 BOTTLE in 1 CARTON (64980-513-15) / 15 mL in 1 BOTTLE
ANDAANDA077259
FDA SPL set id804336
LabelerRising Pharma Holdings, Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2014-12-15
Marketing statusACTIVE

NDC item 68682081205

NDC 968682-812
NDC 1068682-812-05
NDC Item68682081205
packaging1 BOTTLE, DISPENSING in 1 CARTON (68682-812-05) / 5 mL in 1 BOTTLE, DISPENSING
FDA SPL set id657377
LabelerOceanside Pharmaceuticals
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryNDA AUTHORIZED GENERIC
Marketing effective time low2020-06-01
Marketing statusACTIVE
NDA_AUTHORIZED_GENERICNDA018086

NDC item 70069070101

NDC 970069-701
NDC 1070069-701-01
NDC Item70069070101
packaging1 BOTTLE in 1 CARTON (70069-701-01) / 5 mL in 1 BOTTLE
ANDAANDA217764
FDA SPL set id795204
LabelerSomerset Therapeutics, LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2024-07-04
Marketing statusACTIVE

NDC item 70069070201

NDC 970069-702
NDC 1070069-702-01
NDC Item70069070201
packaging1 BOTTLE in 1 CARTON (70069-702-01) / 10 mL in 1 BOTTLE
ANDAANDA217764
FDA SPL set id795204
LabelerSomerset Therapeutics, LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2024-07-04
Marketing statusACTIVE

NDC item 70069070301

NDC 970069-703
NDC 1070069-703-01
NDC Item70069070301
packaging1 BOTTLE in 1 CARTON (70069-703-01) / 15 mL in 1 BOTTLE
ANDAANDA217764
FDA SPL set id795204
LabelerSomerset Therapeutics, LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2024-07-04
Marketing statusACTIVE

NDC item 70756065415

NDC 970756-654
NDC 1070756-654-15
NDC Item70756065415
packaging1 BOTTLE, DROPPER in 1 CARTON (70756-654-15) / 5 mL in 1 BOTTLE, DROPPER
ANDAANDA078771
FDA SPL set id717503
LabelerLifestar Pharma LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2023-06-26
Marketing statusACTIVE

NDC item 70756065530

NDC 970756-655
NDC 1070756-655-30
NDC Item70756065530
packaging1 BOTTLE, DROPPER in 1 CARTON (70756-655-30) / 10 mL in 1 BOTTLE, DROPPER
ANDAANDA078771
FDA SPL set id717503
LabelerLifestar Pharma LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2023-06-26
Marketing statusACTIVE

NDC item 81469020905

NDC 981469-209
NDC 1081469-209-05
NDC Item81469020905
packaging1 BOTTLE, DROPPER in 1 CARTON (81469-209-05) / 5 mL in 1 BOTTLE, DROPPER
ANDAANDA078771
FDA SPL set id785224
LabelerFirst Nation Group, LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2024-05-10
Marketing statusACTIVE

NDC item 81469020910

NDC 981469-209
NDC 1081469-209-10
NDC Item81469020910
packaging1 BOTTLE, DROPPER in 1 CARTON (81469-209-10) / 10 mL in 1 BOTTLE, DROPPER
ANDAANDA078771
FDA SPL set id785224
LabelerFirst Nation Group, LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2024-05-10
Marketing statusACTIVE

NDC item 82260081205

NDC 982260-812
NDC 1082260-812-05
NDC Item82260081205
packaging1 BOTTLE, DISPENSING in 1 CARTON (82260-812-05) / 5 mL in 1 BOTTLE, DISPENSING
FDA SPL set id863431
LabelerBausch & Lomb Americas Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryNDA AUTHORIZED GENERIC
Marketing effective time low2020-06-01
Marketing statusACTIVE
NDA_AUTHORIZED_GENERICNDA018086