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"0378-5036-05" National Drug Code (NDC)
Finasteride 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-5036-05)
(Mylan Pharmaceuticals Inc.)
NDC Code
0378-5036-05
Package Description
500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-5036-05)
Product NDC
0378-5036
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Finasteride
Non-Proprietary Name
Finasteride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20151020
End Marketing Date
20190630
Marketing Category Name
ANDA
Application Number
ANDA077578
Manufacturer
Mylan 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/0378-5036-05