NDC 58118-2279

NDC 58118-2279

NDC 58118-2279 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 58118-2279
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 58118-2279-8 [58118227908]

Amlodipine Besylate and Benazepril Hydrochloride CAPSULE
Marketing CategoryNDA authorized generic
Application NumberNDA020364
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1995-03-03
Marketing End Date2016-09-08

NDC 58118-2279-3 [58118227903]

Amlodipine Besylate and Benazepril Hydrochloride CAPSULE
Marketing CategoryNDA authorized generic
Application NumberNDA020364
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1995-03-03
Marketing End Date2016-09-08

NDC 58118-2279-9 [58118227909]

Amlodipine Besylate and Benazepril Hydrochloride CAPSULE
Marketing CategoryNDA authorized generic
Application NumberNDA020364
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1995-03-03
Marketing End Date2016-09-08

NDC 58118-2279-0 [58118227900]

Amlodipine Besylate and Benazepril Hydrochloride CAPSULE
Marketing CategoryNDA authorized generic
Application NumberNDA020364
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1995-03-03
Marketing End Date2016-09-08

Drug Details

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