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"0006-0071-54" National Drug Code (NDC)
Propecia 90 TABLET, FILM COATED in 1 BOTTLE (0006-0071-54)
(Merck Sharp & Dohme Corp.)
NDC Code
0006-0071-54
Package Description
90 TABLET, FILM COATED in 1 BOTTLE (0006-0071-54)
Product NDC
0006-0071
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Propecia
Non-Proprietary Name
Finasteride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
19971219
Marketing Category Name
NDA
Application Number
NDA020788
Manufacturer
Merck Sharp & Dohme Corp.
Substance Name
FINASTERIDE
Strength
1
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/0006-0071-54