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"68382-169-10" National Drug Code (NDC)

Benazepril Hydrochloride 1000 TABLET, FILM COATED in 1 BOTTLE (68382-169-10)
(Zydus Pharmaceuticals (USA) Inc.)

NDC Code68382-169-10
Package Description1000 TABLET, FILM COATED in 1 BOTTLE (68382-169-10)
Product NDC68382-169
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
Strength5
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/68382-169-10





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