NDC 68788-6875 – Finasteride

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

Human Prescription Drug

Product NDC68788-6875

Product details

Brand name
Finasteride
Generic name
Finasteride
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA203687
Marketed since
January 23, 2017
Listing expires
December 31, 2027
Pharmacologic class
5-alpha Reductase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Finasteride →

Package NDC codes (3)

Package NDCDescriptionSince
68788-6875-330 TABLET, FILM COATED in 1 BOTTLE (68788-6875-3)Jan 23, 2017
68788-6875-660 TABLET, FILM COATED in 1 BOTTLE (68788-6875-6)Jan 23, 2017
68788-6875-990 TABLET, FILM COATED in 1 BOTTLE (68788-6875-9)Jan 23, 2017

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