NDC 16590-115

NDC 16590-115

NDC 16590-115 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 16590-115
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 16590-115-71 [16590011571]

HYDROCODONE BITARTRATE AND ACETAMINOPHEN TABLET
Marketing CategoryANDA
Application NumberANDA081080
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1991-08-30
Inactivation Date2019-11-13

NDC 16590-115-28 [16590011528]

HYDROCODONE BITARTRATE AND ACETAMINOPHEN TABLET
Marketing CategoryANDA
Application NumberANDA081080
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1991-08-30
Inactivation Date2019-11-13

NDC 16590-115-30 [16590011530]

HYDROCODONE BITARTRATE AND ACETAMINOPHEN TABLET
Marketing CategoryANDA
Application NumberANDA081080
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1991-08-30
Inactivation Date2019-11-13

NDC 16590-115-60 [16590011560]

HYDROCODONE BITARTRATE AND ACETAMINOPHEN TABLET
Marketing CategoryANDA
Application NumberANDA081080
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1991-08-30
Inactivation Date2019-11-13

NDC 16590-115-56 [16590011556]

HYDROCODONE BITARTRATE AND ACETAMINOPHEN TABLET
Marketing CategoryANDA
Application NumberANDA081080
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1991-08-30
Inactivation Date2019-11-13

NDC 16590-115-45 [16590011545]

HYDROCODONE BITARTRATE AND ACETAMINOPHEN TABLET
Marketing CategoryANDA
Application NumberANDA081080
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1991-08-30
Inactivation Date2019-11-13

NDC 16590-115-90 [16590011590]

HYDROCODONE BITARTRATE AND ACETAMINOPHEN TABLET
Marketing CategoryANDA
Application NumberANDA081080
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date1991-08-30
Inactivation Date2019-11-13

Drug Details

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.