NDC 68788-8433 – Finasteride

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

Human Prescription Drug

Product NDC68788-8433

Product details

Brand name
Finasteride
Generic name
Finasteride
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA204304
Marketed since
April 24, 2024
Listing expires
December 31, 2026
Pharmacologic class
5-alpha Reductase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Finasteride →

Package NDC codes (4)

Package NDCDescriptionSince
68788-8433-1100 TABLET, FILM COATED in 1 BOTTLE (68788-8433-1)Apr 24, 2024
68788-8433-330 TABLET, FILM COATED in 1 BOTTLE (68788-8433-3)Apr 24, 2024
68788-8433-660 TABLET, FILM COATED in 1 BOTTLE (68788-8433-6)Apr 24, 2024
68788-8433-990 TABLET, FILM COATED in 1 BOTTLE (68788-8433-9)Apr 24, 2024

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