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"0185-0820-05" National Drug Code (NDC)
Benazepril Hydrochloride 500 TABLET, FILM COATED in 1 BOTTLE (0185-0820-05)
(Eon Labs, Inc.)
NDC Code
0185-0820-05
Package Description
500 TABLET, FILM COATED in 1 BOTTLE (0185-0820-05)
Product NDC
0185-0820
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
End Marketing Date
20211031
Marketing Category Name
ANDA
Application Number
ANDA076402
Manufacturer
Eon Labs, 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/0185-0820-05