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"68788-7248-8" National Drug Code (NDC)
Benazepril Hydrochloride 120 TABLET, FILM COATED in 1 BOTTLE (68788-7248-8)
(Preferred Pharmaceuticals Inc.)
NDC Code
68788-7248-8
Package Description
120 TABLET, FILM COATED in 1 BOTTLE (68788-7248-8)
Product NDC
68788-7248
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
20180827
Marketing Category Name
ANDA
Application Number
ANDA078212
Manufacturer
Preferred Pharmaceuticals 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/68788-7248-8