NDC 63304-830 – Atorvastatin Calcium

Atorvastatin Calcium Trihydrate 80 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 6 recalls

Product NDC63304-830

Product details

Brand name
Atorvastatin Calcium
Generic name
Atorvastatin Calcium
Labeler
Sun Pharmaceutical Industries Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA076477
Marketed since
December 1, 2011
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 (2)

Package NDCDescriptionSince
63304-830-05500 TABLET, FILM COATED in 1 BOTTLE (63304-830-05)Dec 1, 2011
63304-830-9090 TABLET, FILM COATED in 1 BOTTLE (63304-830-90)Dec 1, 2011

Recalls mentioning this NDC

Other Atorvastatin Calcium products