NDC 68071-3993 – Finasteride

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

Human Prescription Drug

Product NDC68071-3993

Product details

Brand name
Finasteride
Generic name
Finasteride
Labeler
NuCare Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA203687
Marketed since
November 5, 2013
Listing expires
December 31, 2027
Pharmacologic class
5-alpha Reductase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Finasteride →

Package NDC codes (1)

Package NDCDescriptionSince
68071-3993-330 TABLET, FILM COATED in 1 BOTTLE (68071-3993-3)May 6, 2026

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