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"70934-983-30" National Drug Code (NDC)
Benazepril Hydrochloride 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-983-30)
(Denton Pharma, Inc. DBA Northwind Pharmaceuticals)
NDC Code
70934-983-30
Package Description
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-983-30)
Product NDC
70934-983
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
20220628
End Marketing Date
20231231
Marketing Category Name
ANDA
Application Number
ANDA078212
Manufacturer
Denton Pharma, Inc. DBA Northwind Pharmaceuticals
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/70934-983-30