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"71335-0281-4" National Drug Code (NDC)
Finasteride 28 TABLET, FILM COATED in 1 BOTTLE (71335-0281-4)
(Bryant Ranch Prepack)
NDC Code
71335-0281-4
Package Description
28 TABLET, FILM COATED in 1 BOTTLE (71335-0281-4)
Product NDC
71335-0281
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Finasteride
Non-Proprietary Name
Finasteride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20140920
Marketing Category Name
ANDA
Application Number
ANDA203687
Manufacturer
Bryant Ranch Prepack
Substance Name
FINASTERIDE
Strength
1
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/71335-0281-4