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"17856-0090-1" National Drug Code (NDC)
Finasteride 1 TABLET, FILM COATED in 1 POUCH (17856-0090-1)
(Atlantic Biologicals Corps)
NDC Code
17856-0090-1
Package Description
1 TABLET, FILM COATED in 1 POUCH (17856-0090-1)
Product NDC
17856-0090
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Finasteride
Non-Proprietary Name
Finasteride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20100528
Marketing Category Name
ANDA
Application Number
ANDA090121
Manufacturer
Atlantic Biologicals Corps
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/17856-0090-1