NDC 60505-2579 – Atorvastatin Calcium

Atorvastatin Calcium Propylene Glycol Solvate 20 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 1 recall

Product NDC60505-2579

Product details

Brand name
Atorvastatin Calcium
Generic name
Atorvastatin Calcium
Labeler
Apotex Corp.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090548
Marketed since
May 29, 2012
Listing expires
December 31, 2027
Pharmacologic class
HMG-CoA Reductase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Atorvastatin Calcium →

Package NDC codes (6)

Package NDCDescriptionSince
60505-2579-010 BLISTER PACK in 1 CARTON (60505-2579-0) / 10 TABLET, FILM COATED in 1 BLISTER PACKMay 29, 2012
60505-2579-330 TABLET, FILM COATED in 1 BOTTLE (60505-2579-3)May 29, 2012
60505-2579-5500 TABLET, FILM COATED in 1 BOTTLE (60505-2579-5)May 29, 2012
60505-2579-75000 TABLET, FILM COATED in 1 BOTTLE (60505-2579-7)May 29, 2012
60505-2579-81000 TABLET, FILM COATED in 1 BOTTLE (60505-2579-8)May 29, 2012
60505-2579-990 TABLET, FILM COATED in 1 BOTTLE (60505-2579-9)May 29, 2012

Recalls mentioning this NDC

Other Atorvastatin Calcium products