NDC 42549-652

NDC 42549-652

NDC 42549-652 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 42549-652
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 42549-652-40 [42549065240]

Methocarbamol TABLET
Marketing CategoryANDA
Application NumberANDA084277
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1987-11-01
Inactivation Date2019-11-13

NDC 42549-652-60 [42549065260]

Methocarbamol TABLET
Marketing CategoryANDA
Application NumberANDA084277
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1987-11-01
Inactivation Date2019-11-13

NDC 42549-652-30 [42549065230]

Methocarbamol TABLET
Marketing CategoryANDA
Application NumberANDA084277
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1987-11-01
Inactivation Date2019-11-13

NDC 42549-652-81 [42549065281]

Methocarbamol TABLET
Marketing CategoryANDA
Application NumberANDA084277
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1987-11-01
Inactivation Date2019-11-13

NDC 42549-652-12 [42549065212]

Methocarbamol TABLET
Marketing CategoryANDA
Application NumberANDA084277
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1987-11-01
Inactivation Date2019-11-13

NDC 42549-652-90 [42549065290]

Methocarbamol TABLET
Marketing CategoryANDA
Application NumberANDA084277
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1987-11-01
Inactivation Date2019-11-13

Drug Details


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