NDC 58118-0164

NDC 58118-0164

NDC 58118-0164 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 58118-0164
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 58118-0164-0 [58118016400]

Carvedilol TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078251
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2007-09-05
Marketing End Date2016-12-09

NDC 58118-0164-3 [58118016403]

Carvedilol TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078251
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2007-09-05
Marketing End Date2016-12-09

NDC 58118-0164-8 [58118016408]

Carvedilol TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078251
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2007-09-05
Marketing End Date2018-12-01

NDC 58118-0164-9 [58118016409]

Carvedilol TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078251
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2007-09-05
Marketing End Date2016-12-09

Drug Details


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