NDC 31722-525 – Finasteride

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

Human Prescription Drug 1 recall

Product NDC31722-525

Product details

Brand name
Finasteride
Generic name
Finasteride
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090061
Marketed since
June 13, 2015
Listing expires
December 31, 2026
Pharmacologic class
5-alpha Reductase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Finasteride →

Package NDC codes (5)

Package NDCDescriptionSince
31722-525-01100 TABLET, FILM COATED in 1 BOTTLE (31722-525-01)Jun 13, 2015
31722-525-05500 TABLET, FILM COATED in 1 BOTTLE (31722-525-05)Jun 13, 2015
31722-525-101000 TABLET, FILM COATED in 1 BOTTLE (31722-525-10)Jun 13, 2015
31722-525-3012 BOTTLE in 1 CASE (31722-525-30) / 30 TABLET, FILM COATED in 1 BOTTLEJun 13, 2015
31722-525-9012 BOTTLE in 1 CASE (31722-525-90) / 90 TABLET, FILM COATED in 1 BOTTLEJun 13, 2015

Recalls mentioning this NDC

Other Finasteride products