NDC 68788-8377 – Finasteride

Finasteride 5 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC68788-8377

Product details

Brand name
Finasteride
Generic name
Finasteride
Labeler
Preferred Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090061
Marketed since
February 28, 2023
Listing expires
December 31, 2027
Pharmacologic class
5-alpha Reductase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Finasteride →

Package NDC codes (4)

Package NDCDescriptionSince
68788-8377-1100 TABLET, FILM COATED in 1 BOTTLE (68788-8377-1)Feb 28, 2023
68788-8377-330 TABLET, FILM COATED in 1 BOTTLE (68788-8377-3)Feb 28, 2023
68788-8377-660 TABLET, FILM COATED in 1 BOTTLE (68788-8377-6)Feb 28, 2023
68788-8377-990 TABLET, FILM COATED in 1 BOTTLE (68788-8377-9)Feb 28, 2023

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