RxSearch
HomeSearchNDC id 1922783

NDC properties for NDC 9 42571-382

NDC item 42571038227

NDC 942571-382
NDC 1042571-382-27
NDC Item42571038227
packaging12 POUCH in 1 CARTON (42571-382-27) / 15 VIAL, SINGLE-USE in 1 POUCH / .2 mL in 1 VIAL, SINGLE-USE
ANDAANDA215936
LabelerMicro Labs Limited
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2022-02-15
Marketing statusACTIVE

NDC item 42571038271

NDC 942571-382
NDC 1042571-382-71
NDC Item42571038271
packaging0.2 mL in 1 VIAL, SINGLE-USE
packaging15 in 1 POUCH
ANDAANDA215936
LabelerMicro Labs Limited
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2022-02-15
Marketing statusACTIVE

NDC item 42571038273

NDC 942571-382
NDC 1042571-382-73
NDC Item42571038273
packaging4 POUCH in 1 CARTON (42571-382-73) / 15 VIAL, SINGLE-USE in 1 POUCH (42571-382-71) / .2 mL in 1 VIAL, SINGLE-USE
ANDAANDA215936
LabelerMicro Labs Limited
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2022-02-15
Marketing statusACTIVE

NDC item 50383026161

NDC 950383-261
NDC 1050383-261-61
NDC Item50383026161
packaging4 POUCH in 1 CARTON (50383-261-61) / 15 VIAL, SINGLE-USE in 1 POUCH / .2 mL in 1 VIAL, SINGLE-USE
LabelerAkorn
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryNDA
Marketing effective time low2019-02-01
Marketing statusACTIVE
NDANDA202667

NDC item 50383026191

NDC 950383-261
NDC 1050383-261-91
NDC Item50383026191
packaging12 POUCH in 1 CARTON (50383-261-91) / 15 VIAL, SINGLE-USE in 1 POUCH / .2 mL in 1 VIAL, SINGLE-USE
LabelerAkorn Operating Company LLC (dba Akorn)
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryNDA
Marketing effective time low2019-02-01
Marketing statusACTIVE
NDANDA202667

NDC item 50742032305

NDC 950742-323
NDC 1050742-323-05
NDC Item50742032305
packaging0.2 mL in 1 VIAL
packaging5 in 1 POUCH
ANDAANDA217260
LabelerIngenus Pharmaceuticals, LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2023-05-02
Marketing statusACTIVE

NDC item 50742032360

NDC 950742-323
NDC 1050742-323-60
NDC Item50742032360
packaging12 POUCH in 1 CARTON (50742-323-60) / 5 VIAL in 1 POUCH (50742-323-05) / .2 mL in 1 VIAL
ANDAANDA217260
LabelerIngenus Pharmaceuticals, LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2023-05-02
Marketing statusACTIVE

NDC item 65862094715

NDC 965862-947
NDC 1065862-947-15
NDC Item65862094715
packaging0.2 mL in 1 VIAL, SINGLE-USE
packaging15 in 1 POUCH
ANDAANDA207630
LabelerAurobindo Pharma Limited
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2018-07-24
Marketing statusACTIVE

NDC item 65862094718

NDC 965862-947
NDC 1065862-947-18
NDC Item65862094718
packaging12 POUCH in 1 CARTON (65862-947-18) / 15 VIAL, SINGLE-USE in 1 POUCH / .2 mL in 1 VIAL, SINGLE-USE
ANDAANDA207630
LabelerAurobindo Pharma Limited
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2018-07-24
Marketing statusACTIVE

NDC item 65862094760

NDC 965862-947
NDC 1065862-947-60
NDC Item65862094760
packaging4 POUCH in 1 CARTON (65862-947-60) / 15 VIAL, SINGLE-USE in 1 POUCH (65862-947-15) / .2 mL in 1 VIAL, SINGLE-USE
ANDAANDA207630
LabelerAurobindo Pharma Limited
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2018-07-24
Marketing statusACTIVE

NDC item 72162238706

NDC 972162-2387
NDC 1072162-2387-6
NDC Item72162238706
packaging4 POUCH in 1 CARTON (72162-2387-6) / 15 VIAL, SINGLE-USE in 1 POUCH (72162-2387-7) / .2 mL in 1 VIAL, SINGLE-USE
ANDAANDA215936
LabelerBryant Ranch Prepack
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2022-02-15
Marketing statusACTIVE

NDC item 72162238707

NDC 972162-2387
NDC 1072162-2387-7
NDC Item72162238707
packaging0.2 mL in 1 VIAL, SINGLE-USE
packaging15 in 1 POUCH
ANDAANDA215936
LabelerBryant Ranch Prepack
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2022-02-15
Marketing statusACTIVE