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"50742-123-90" National Drug Code (NDC)
Finasteride 90 TABLET, FILM COATED in 1 BOTTLE (50742-123-90)
(Ingenus Pharmaceuticals, LLC)
NDC Code
50742-123-90
Package Description
90 TABLET, FILM COATED in 1 BOTTLE (50742-123-90)
Product NDC
50742-123
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Finasteride
Non-Proprietary Name
Finasteride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20110801
Marketing Category Name
ANDA
Application Number
ANDA090121
Manufacturer
Ingenus Pharmaceuticals, LLC
Substance Name
FINASTERIDE
Strength
5
Strength Unit
mg/1
Pharmacy Classes
5-alpha Reductase Inhibitor [EPC],5-alpha Reductase Inhibitors [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/50742-123-90