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"51079-321-20" National Drug Code (NDC)
Finasteride 100 BLISTER PACK in 1 CARTON (51079-321-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-321-01)
(Mylan Institutional Inc.)
NDC Code
51079-321-20
Package Description
100 BLISTER PACK in 1 CARTON (51079-321-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-321-01)
Product NDC
51079-321
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Finasteride
Non-Proprietary Name
Finasteride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20150713
End Marketing Date
20190630
Marketing Category Name
ANDA
Application Number
ANDA077578
Manufacturer
Mylan Institutional Inc.
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/51079-321-20