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NDC properties for NDC 9 17478-189

NDC item 17478018924

NDC 917478-189
NDC 1017478-189-24
NDC Item17478018924
packaging12 VIAL, SINGLE-DOSE in 1 CARTON (17478-189-24) / .3 mL in 1 VIAL, SINGLE-DOSE
ANDAANDA212291
FDA SPL set id656785
LabelerAkorn Operating Company LLC (dba Akorn)
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing statusACTIVE

NDC item 24208049605

NDC 924208-496
NDC 1024208-496-05
NDC Item24208049605
packaging4 POUCH in 1 CARTON (24208-496-05) / 15 CONTAINER in 1 POUCH / .3 mL in 1 CONTAINER
FDA SPL set id554526
LabelerBAUSCH & LOMB INCORPORATED
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryNDA AUTHORIZED GENERIC
Marketing effective time low2021-03-16
Marketing statusACTIVE
NDA_AUTHORIZED_GENERICNDA019463

NDC item 42571039871

NDC 942571-398
NDC 1042571-398-71
NDC Item42571039871
packaging6 POUCH in 1 CARTON (42571-398-71) / 10 VIAL in 1 POUCH / .3 mL in 1 VIAL
ANDAANDA216596
FDA SPL set id837331
LabelerMicro Labs Limited
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2023-01-01
Marketing statusACTIVE

NDC item 50742028804

NDC 950742-288
NDC 1050742-288-04
NDC Item50742028804
packaging0.3 mL in 1 CONTAINER
packaging4 in 1 POUCH
ANDAANDA216533
FDA SPL set id749629
LabelerIngenus Pharmaceuticals, LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2022-09-15
Marketing statusACTIVE

NDC item 50742028860

NDC 950742-288
NDC 1050742-288-60
NDC Item50742028860
packaging15 POUCH in 1 CARTON (50742-288-60) / 4 CONTAINER in 1 POUCH (50742-288-04) / .3 mL in 1 CONTAINER
ANDAANDA216533
FDA SPL set id749629
LabelerIngenus Pharmaceuticals, LLC
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2022-09-15
Marketing statusACTIVE

NDC item 69918060160

NDC 969918-601
NDC 1069918-601-60
NDC Item69918060160
packaging60 POUCH in 1 CARTON (69918-601-60) / 10 CONTAINER in 1 POUCH / .3 mL in 1 CONTAINER
ANDAANDA212592
FDA SPL set id623687
LabelerNordic Pharma, Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2022-02-26
Marketing statusACTIVE

NDC item 72485060205

NDC 972485-602
NDC 1072485-602-05
NDC Item72485060205
packaging0.3 mL in 1 VIAL
packaging10 in 1 POUCH
ANDAANDA217195
COLORTEXTYellow(light yellow)
ColorC48330 __
FDA SPL set id841421
LabelerArmas Pharmaceuticals, Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2023-05-08
Marketing statusACTIVE

NDC item 72485060260

NDC 972485-602
NDC 1072485-602-60
NDC Item72485060260
packaging6 POUCH in 1 CARTON (72485-602-60) / 10 VIAL in 1 POUCH (72485-602-05) / .3 mL in 1 VIAL
ANDAANDA217195
COLORTEXTYellow(light yellow)
ColorC48330 __
FDA SPL set id841421
LabelerArmas Pharmaceuticals, Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryANDA
Marketing effective time low2023-05-08
Marketing statusACTIVE

NDC item 82260049605

NDC 982260-496
NDC 1082260-496-05
NDC Item82260049605
packaging6 POUCH in 1 CARTON (82260-496-05) / 10 CONTAINER in 1 POUCH / .3 mL in 1 CONTAINER
FDA SPL set id863545
LabelerBausch & Lomb Americas Inc.
Label typeHUMAN PRESCRIPTION DRUG
Marketing categoryNDA AUTHORIZED GENERIC
Marketing effective time low2022-02-17
Marketing statusACTIVE
NDA_AUTHORIZED_GENERICNDA019463