NDC 31722-514 – Simvastatin

Simvastatin 80 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 1 recall

Product NDC31722-514

Product details

Brand name
Simvastatin
Generic name
Simvastatin
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA200895
Marketed since
December 9, 2014
Listing expires
December 31, 2026
Pharmacologic class
HMG-CoA Reductase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Simvastatin →

Package NDC codes (4)

Package NDCDescriptionSince
31722-514-01100 TABLET, FILM COATED in 1 BOTTLE (31722-514-01)Dec 9, 2014
31722-514-05500 TABLET, FILM COATED in 1 BOTTLE (31722-514-05)Dec 9, 2014
31722-514-3030 TABLET, FILM COATED in 1 BOTTLE (31722-514-30)Dec 9, 2014
31722-514-9090 TABLET, FILM COATED in 1 BOTTLE (31722-514-90)Dec 9, 2014

Recalls mentioning this NDC

Other Simvastatin products