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"68382-172-16" National Drug Code (NDC)

Benazepril Hydrochloride 90 TABLET, FILM COATED in 1 BOTTLE (68382-172-16)
(Zydus Pharmaceuticals (USA) Inc.)

NDC Code68382-172-16
Package Description90 TABLET, FILM COATED in 1 BOTTLE (68382-172-16)
Product NDC68382-172
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameBenazepril Hydrochloride
Non-Proprietary NameBenazepril Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20171113
Marketing Category NameANDA
Application NumberANDA078848
ManufacturerZydus Pharmaceuticals (USA) Inc.
Substance NameBENAZEPRIL HYDROCHLORIDE
Strength40
Strength Unitmg/1
Pharmacy ClassesAngiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE]

Find more : http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/68382-172-16





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