NDC 63874-861

NDC 63874-861

NDC 63874-861 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 63874-861
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 63874-861-30 [63874086130]

Hydrocodone Bitartrate And Acetaminophen TABLET
Marketing CategoryANDA
Application NumberANDA040143
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2010-01-01
Inactivation Date2019-10-21

NDC 63874-861-60 [63874086160]

Hydrocodone Bitartrate And Acetaminophen TABLET
Marketing CategoryANDA
Application NumberANDA040143
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2010-01-01
Inactivation Date2019-10-21

NDC 63874-861-01 [63874086101]

Hydrocodone Bitartrate And Acetaminophen TABLET
Marketing CategoryANDA
Application NumberANDA040143
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2010-01-01
Inactivation Date2019-10-21

NDC 63874-861-90 [63874086190]

Hydrocodone Bitartrate And Acetaminophen TABLET
Marketing CategoryANDA
Application NumberANDA040143
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2010-01-01
Inactivation Date2019-10-21

Drug Details

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.