NDC 68071-3094 – Finasteride

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

Human Prescription Drug

Product NDC68071-3094

Product details

Brand name
Finasteride
Generic name
Finasteride
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090060
Marketed since
July 1, 2013
Listing expires
December 31, 2026
Pharmacologic class
5-alpha Reductase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Finasteride →

Package NDC codes (1)

Package NDCDescriptionSince
68071-3094-330 TABLET, FILM COATED in 1 BOTTLE (68071-3094-3)Aug 2, 2019

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