NDC 58118-2272

NDC 58118-2272

NDC 58118-2272 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 58118-2272
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 58118-2272-9 [58118227209]

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 58118-2272-3 [58118227203]

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 58118-2272-0 [58118227200]

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 58118-2272-8 [58118227208]

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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