NDC 31722-526 – Finasteride

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

Human Prescription Drug

Product NDC31722-526

Product details

Brand name
Finasteride
Generic name
Finasteride
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090060
Marketed since
July 1, 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 (3)

Package NDCDescriptionSince
31722-526-101000 TABLET, FILM COATED in 1 BOTTLE (31722-526-10)Jul 1, 2013
31722-526-3030 TABLET, FILM COATED in 1 BOTTLE (31722-526-30)Jul 1, 2013
31722-526-9090 TABLET, FILM COATED in 1 BOTTLE (31722-526-90)Jul 1, 2013

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