NDC 71335-1051 – Atorvastatin Calcium

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

Human Prescription Drug

Product NDC71335-1051

Product details

Brand name
Atorvastatin Calcium
Generic name
Atorvastatin Calcium
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA090548
Marketed since
May 29, 2012
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 (9)

Package NDCDescriptionSince
71335-1051-130 TABLET, FILM COATED in 1 BOTTLE (71335-1051-1)Jan 4, 2019
71335-1051-260 TABLET, FILM COATED in 1 BOTTLE (71335-1051-2)Dec 9, 2024
71335-1051-390 TABLET, FILM COATED in 1 BOTTLE (71335-1051-3)Feb 6, 2019
71335-1051-49 TABLET, FILM COATED in 1 BOTTLE (71335-1051-4)Dec 9, 2024
71335-1051-528 TABLET, FILM COATED in 1 BOTTLE (71335-1051-5)Dec 9, 2024
71335-1051-620 TABLET, FILM COATED in 1 BOTTLE (71335-1051-6)Dec 9, 2024
71335-1051-7180 TABLET, FILM COATED in 1 BOTTLE (71335-1051-7)Dec 9, 2024
71335-1051-8100 TABLET, FILM COATED in 1 BOTTLE (71335-1051-8)Dec 9, 2024
71335-1051-97 TABLET, FILM COATED in 1 BOTTLE (71335-1051-9)Dec 9, 2024

Other Atorvastatin Calcium products