NDC 63874-293

NDC 63874-293

NDC 63874-293 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 63874-293
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 63874-293-60 [63874029360]

Hydrocodone Bitartrate And Acetaminophen TABLET
Marketing CategoryANDA
Application NumberANDA040356
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2010-01-01
Inactivation Date2019-10-21

NDC 63874-293-90 [63874029390]

Hydrocodone Bitartrate And Acetaminophen TABLET
Marketing CategoryANDA
Application NumberANDA040356
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2010-01-01
Inactivation Date2019-10-21

NDC 63874-293-01 [63874029301]

Hydrocodone Bitartrate And Acetaminophen TABLET
Marketing CategoryANDA
Application NumberANDA040356
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2010-01-01
Inactivation Date2019-10-21

NDC 63874-293-30 [63874029330]

Hydrocodone Bitartrate And Acetaminophen TABLET
Marketing CategoryANDA
Application NumberANDA040356
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.