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"63739-495-40" National Drug Code (NDC)
Finasteride 100 TABLET, FILM COATED in 1 BOTTLE (63739-495-40)
(McKesson Packaging Services Business Unit of McKesson Corporation)
NDC Code
63739-495-40
Package Description
100 TABLET, FILM COATED in 1 BOTTLE (63739-495-40)
Product NDC
63739-495
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Finasteride
Non-Proprietary Name
Finasteride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20101122
Marketing Category Name
ANDA
Application Number
ANDA077914
Manufacturer
McKesson Packaging Services Business Unit of McKesson Corporation
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/63739-495-40