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"61919-739-90" National Drug Code (NDC)
Benazepril 90 TABLET, COATED in 1 BOTTLE (61919-739-90)
(Direct_Rx)
NDC Code
61919-739-90
Package Description
90 TABLET, COATED in 1 BOTTLE (61919-739-90)
Product NDC
61919-739
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Benazepril
Non-Proprietary Name
Benazepril
Dosage Form
TABLET, COATED
Usage
ORAL
Start Marketing Date
20190115
Marketing Category Name
ANDA
Application Number
ANDA076118
Manufacturer
Direct_Rx
Substance Name
BENAZEPRIL HYDROCHLORIDE
Strength
20
Strength Unit
mg/1
Pharmacy Classes
Angiotensin 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/61919-739-90