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"68071-1969-2" National Drug Code (NDC)
Benazepril Hydrochloride 120 TABLET, COATED in 1 BOTTLE (68071-1969-2)
(NuCare Pharmaceuticals,Inc.)
NDC Code
68071-1969-2
Package Description
120 TABLET, COATED in 1 BOTTLE (68071-1969-2)
Product NDC
68071-1969
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Benazepril Hydrochloride
Non-Proprietary Name
Benazepril Hydrochloride
Dosage Form
TABLET, COATED
Usage
ORAL
Start Marketing Date
20140101
Marketing Category Name
ANDA
Application Number
ANDA076118
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/68071-1969-2