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"71335-1086-5" National Drug Code (NDC)
Benazepril Hydrochloride 14 TABLET in 1 BOTTLE (71335-1086-5)
(Bryant Ranch Prepack)
NDC Code
71335-1086-5
Package Description
14 TABLET in 1 BOTTLE (71335-1086-5)
Product NDC
71335-1086
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Benazepril Hydrochloride
Non-Proprietary Name
Benazepril Hydrochloride
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20100202
Marketing Category Name
ANDA
Application Number
ANDA076820
Manufacturer
Bryant Ranch Prepack
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/71335-1086-5