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"61786-669-02" National Drug Code (NDC)
Benazepril Hydrochloride 30 TABLET in 1 BOTTLE (61786-669-02)
(REMEDYREPACK INC.)
NDC Code
61786-669-02
Package Description
30 TABLET in 1 BOTTLE (61786-669-02)
Product NDC
61786-669
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Benazepril Hydrochloride
Non-Proprietary Name
Benazepril Hydrochloride
Dosage Form
TABLET
Usage
ORAL
Start Marketing Date
20160504
Marketing Category Name
ANDA
Application Number
ANDA076820
Manufacturer
REMEDYREPACK INC.
Substance Name
BENAZEPRIL HYDROCHLORIDE
Strength
10
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/61786-669-02