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"68788-8749-1" National Drug Code (NDC)
Finasteride 100 TABLET, FILM COATED in 1 BOTTLE (68788-8749-1)
(Preferred Pharmaceuticals Inc.)
NDC Code
68788-8749-1
Package Description
100 TABLET, FILM COATED in 1 BOTTLE (68788-8749-1)
Product NDC
68788-8749
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Finasteride
Non-Proprietary Name
Finasteride
Dosage Form
TABLET, FILM COATED
Usage
ORAL
Start Marketing Date
20241011
Marketing Category Name
ANDA
Application Number
ANDA078341
Manufacturer
Preferred Pharmaceuticals 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/68788-8749-1