NDC 67877-511 – Atorvastatin Calcium

Atorvastatin Calcium Trihydrate 10 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug 4 recalls

Product NDC67877-511

Product details

Brand name
Atorvastatin Calcium
Generic name
Atorvastatin Calcium
Labeler
Ascend Laboratories, LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA209288
Marketed since
December 23, 2018
Listing expires
December 31, 2026
Pharmacologic class
HMG-CoA Reductase Inhibitor

Active ingredients

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

Package NDC codes (5)

Package NDCDescriptionSince
67877-511-05500 TABLET, FILM COATED in 1 BOTTLE (67877-511-05)Dec 23, 2018
67877-511-101000 TABLET, FILM COATED in 1 BOTTLE (67877-511-10)Dec 23, 2018
67877-511-3810 BLISTER PACK in 1 CARTON (67877-511-38) / 10 TABLET, FILM COATED in 1 BLISTER PACK (67877-511-33)Dec 23, 2018
67877-511-555000 TABLET, FILM COATED in 1 BOTTLE (67877-511-55)Dec 23, 2018
67877-511-9090 TABLET, FILM COATED in 1 BOTTLE (67877-511-90)Dec 23, 2018

Recalls mentioning this NDC

Other Atorvastatin Calcium products