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"35573-400-99" National Drug Code (NDC)
Finasteride 1000 TABLET, FILM COATED in 1 BOTTLE (35573-400-99)
(Burel Pharmaceuticals, LLC)
NDC Code
35573-400-99
Package Description
1000 TABLET, FILM COATED in 1 BOTTLE (35573-400-99)
Product NDC
35573-400
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Finasteride
Non-Proprietary Name
Finasteride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20180713
Marketing Category Name
ANDA
Application Number
ANDA203687
Manufacturer
Burel Pharmaceuticals, LLC
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/35573-400-99