NDC 71335-0802

NDC 71335-0802

NDC 71335-0802 is a in the category. It is labeled and distributed by .

Proprietary NameNDC 71335-0802
Marketing Category/

Packaging

NDC SPL Data Element Entries

NDC 71335-0802-3 [71335080203]

Amlodipine and Benazepril Hydrochloride CAPSULE
Marketing CategoryANDA
Application NumberANDA077890
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-10-15
Marketing End Date2017-12-31

NDC 71335-0802-1 [71335080201]

Amlodipine and Benazepril Hydrochloride CAPSULE
Marketing CategoryANDA
Application NumberANDA077890
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-10-15
Marketing End Date2017-12-31

NDC 71335-0802-2 [71335080202]

Amlodipine and Benazepril Hydrochloride CAPSULE
Marketing CategoryANDA
Application NumberANDA077890
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-10-15
Marketing End Date2017-12-31

Drug Details

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