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"70518-0397-0" National Drug Code (NDC)
Finasteride 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0397-0)
(REMEDYREPACK INC.)
NDC Code
70518-0397-0
Package Description
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0397-0)
Product NDC
70518-0397
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Finasteride
Non-Proprietary Name
Finasteride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20170404
Marketing Category Name
ANDA
Application Number
ANDA090121
Manufacturer
REMEDYREPACK 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/70518-0397-0