NDC 16729-090 – Finasteride

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

Human Prescription Drug 1 recall

Product NDC16729-090

Product details

Brand name
Finasteride
Generic name
finasteride
Labeler
Accord Healthcare, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090121
Marketed since
May 28, 2010
Listing expires
December 31, 2027
Pharmacologic class
5-alpha Reductase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Finasteride →

Package NDC codes (4)

Package NDCDescriptionSince
16729-090-01100 TABLET, FILM COATED in 1 BOTTLE (16729-090-01)Aug 24, 2010
16729-090-1030 TABLET, FILM COATED in 1 BOTTLE (16729-090-10)May 28, 2010
16729-090-1590 TABLET, FILM COATED in 1 BOTTLE (16729-090-15)Jun 8, 2010
16729-090-16500 TABLET, FILM COATED in 1 BOTTLE (16729-090-16)Nov 15, 2011

Recalls mentioning this NDC

Other Finasteride products