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"21695-326-90" National Drug Code (NDC)
Benazepril Hydrochloride 90 TABLET, FILM COATED in 1 BOTTLE (21695-326-90)
(Rebel Distributors Corp.)
NDC Code
21695-326-90
Package Description
90 TABLET, FILM COATED in 1 BOTTLE (21695-326-90)
Product NDC
21695-326
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
20040211
Marketing Category Name
ANDA
Application Number
ANDA076402
Manufacturer
Rebel Distributors Corp.
Substance Name
D&C YELLOW NO. 10
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/21695-326-90