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"59762-0850-2" National Drug Code (NDC)
Finasteride 30 TABLET, FILM COATED in 1 BOTTLE (59762-0850-2)
(Greenstone LLC)
NDC Code
59762-0850-2
Package Description
30 TABLET, FILM COATED in 1 BOTTLE (59762-0850-2)
Product NDC
59762-0850
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Finasteride
Non-Proprietary Name
Finasteride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20071030
End Marketing Date
20160229
Marketing Category Name
ANDA
Application Number
ANDA078341
Manufacturer
Greenstone 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/59762-0850-2