NDC 58118-2271

NDC 58118-2271

NDC 58118-2271 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 58118-2271
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 58118-2271-0 [58118227100]

Amlodipine Besylate and Benazepril Hydrochloride CAPSULE
Marketing CategoryANDA
Application NumberANDA020364
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1995-03-03
Marketing End Date2016-09-08

NDC 58118-2271-9 [58118227109]

Amlodipine Besylate and Benazepril Hydrochloride CAPSULE
Marketing CategoryANDA
Application NumberANDA020364
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1995-03-03
Marketing End Date2016-09-08

NDC 58118-2271-3 [58118227103]

Amlodipine Besylate and Benazepril Hydrochloride CAPSULE
Marketing CategoryANDA
Application NumberANDA020364
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1995-03-03
Marketing End Date2016-09-08

NDC 58118-2271-8 [58118227108]

Amlodipine Besylate and Benazepril Hydrochloride CAPSULE
Marketing CategoryANDA
Application NumberANDA020364
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date1995-03-03
Marketing End Date2016-09-08

Drug Details

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