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"70518-1700-0" National Drug Code (NDC)
Benazepril Hydrochloride 90 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-1700-0)
(REMEDYREPACK INC.)
NDC Code
70518-1700-0
Package Description
90 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-1700-0)
Product NDC
70518-1700
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Benazepril Hydrochloride
Non-Proprietary Name
Benazepril Hydrochloride
Dosage Form
TABLET, COATED
Usage
ORAL
Start Marketing Date
20181129
Marketing Category Name
ANDA
Application Number
ANDA076118
Manufacturer
REMEDYREPACK INC.
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/70518-1700-0