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"76282-412-10" National Drug Code (NDC)
Finasteride 1000 TABLET, FILM COATED in 1 BOTTLE (76282-412-10)
(Exelan Pharmaceuticals Inc.)
NDC Code
76282-412-10
Package Description
1000 TABLET, FILM COATED in 1 BOTTLE (76282-412-10)
Product NDC
76282-412
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Finasteride
Non-Proprietary Name
Finasteride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20150522
Marketing Category Name
ANDA
Application Number
ANDA090061
Manufacturer
Exelan Pharmaceuticals 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/76282-412-10