NDC 71335-0837

NDC 71335-0837

NDC 71335-0837 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 71335-0837
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 71335-0837-1 [71335083701]

Amlodipine and Benazepril Hydrochloride CAPSULE
Marketing CategoryANDA
Application NumberANDA077890
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-05-30
Marketing End Date2018-06-01

NDC 71335-0837-3 [71335083703]

Amlodipine and Benazepril Hydrochloride CAPSULE
Marketing CategoryANDA
Application NumberANDA077890
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-05-30
Marketing End Date2018-06-01

NDC 71335-0837-2 [71335083702]

Amlodipine and Benazepril Hydrochloride CAPSULE
Marketing CategoryANDA
Application NumberANDA077890
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-05-30
Marketing End Date2018-06-01

Drug Details

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