NDC 54868-5650

NDC 54868-5650

NDC 54868-5650 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 54868-5650
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 54868-5650-1 [54868565001]

Meloxicam TABLET
Marketing CategoryANDA
Application NumberANDA077927
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2006-08-07
Inactivation Date2019-09-24

NDC 54868-5650-3 [54868565003]

Meloxicam TABLET
Marketing CategoryANDA
Application NumberANDA077927
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2006-08-07
Inactivation Date2019-09-24

NDC 54868-5650-0 [54868565000]

Meloxicam TABLET
Marketing CategoryANDA
Application NumberANDA077927
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2006-08-07
Inactivation Date2019-09-24

NDC 54868-5650-6 [54868565006]

Meloxicam TABLET
Marketing CategoryANDA
Application NumberANDA077927
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2011-02-22
Inactivation Date2019-09-24

NDC 54868-5650-4 [54868565004]

Meloxicam TABLET
Marketing CategoryANDA
Application NumberANDA077927
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2006-08-07
Inactivation Date2019-09-24

NDC 54868-5650-2 [54868565002]

Meloxicam TABLET
Marketing CategoryANDA
Application NumberANDA077927
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2006-08-07
Inactivation Date2019-09-24

NDC 54868-5650-5 [54868565005]

Meloxicam TABLET
Marketing CategoryANDA
Application NumberANDA077927
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2010-10-01
Inactivation Date2019-09-24

Drug Details

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