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"68071-2929-9" National Drug Code (NDC)
Benazepril Hydrochloride 90 TABLET, FILM COATED in 1 BOTTLE (68071-2929-9)
(NuCare Pharmaceuticals,Inc.)
NDC Code
68071-2929-9
Package Description
90 TABLET, FILM COATED in 1 BOTTLE (68071-2929-9)
Product NDC
68071-2929
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Benazepril Hydrochloride
Non-Proprietary Name
Benazepril Hydrochloride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20080522
Marketing Category Name
ANDA
Application Number
ANDA078212
Manufacturer
NuCare Pharmaceuticals,Inc.
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/68071-2929-9