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"21695-877-90" National Drug Code (NDC)
Benazepril Hydrochloride 90 TABLET, FILM COATED in 1 BOTTLE (21695-877-90)
(Rebel Distributors Corp.)
NDC Code
21695-877-90
Package Description
90 TABLET, FILM COATED in 1 BOTTLE (21695-877-90)
Product NDC
21695-877
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
BENAZEPRIL HYDROCHLORIDE
Strength
40
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/21695-877-90