NDC 58118-0162

NDC 58118-0162

NDC 58118-0162 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 58118-0162
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 58118-0162-3 [58118016203]

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

NDC 58118-0162-6 [58118016206]

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

NDC 58118-0162-8 [58118016208]

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

NDC 58118-0162-9 [58118016209]

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

NDC 58118-0162-0 [58118016200]

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

Drug Details

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