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"58118-7355-3" National Drug Code (NDC)
Finasteride 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (58118-7355-3)
(Clinical Solutions Wholesale)
NDC Code
58118-7355-3
Package Description
30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (58118-7355-3)
Product NDC
58118-7355
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Finasteride
Non-Proprietary Name
Finasteride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20061215
Marketing Category Name
ANDA
Application Number
ANDA076511
Manufacturer
Clinical Solutions Wholesale
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/58118-7355-3