NDC 71335-2799 – Atorvastatin calcium

Atorvastatin Calcium Trihydrate 20 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC71335-2799

Product details

Brand name
Atorvastatin calcium
Generic name
Atorvastatin calcium
Labeler
Bryant Ranch Prepack
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA211933
Marketed since
February 8, 2019
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
71335-2799-130 TABLET, FILM COATED in 1 BOTTLE (71335-2799-1)Oct 13, 2025
71335-2799-260 TABLET, FILM COATED in 1 BOTTLE (71335-2799-2)Oct 13, 2025
71335-2799-390 TABLET, FILM COATED in 1 BOTTLE (71335-2799-3)Oct 13, 2025
71335-2799-49 TABLET, FILM COATED in 1 BOTTLE (71335-2799-4)Oct 13, 2025
71335-2799-528 TABLET, FILM COATED in 1 BOTTLE (71335-2799-5)Oct 13, 2025
71335-2799-620 TABLET, FILM COATED in 1 BOTTLE (71335-2799-6)Oct 13, 2025
71335-2799-7180 TABLET, FILM COATED in 1 BOTTLE (71335-2799-7)Oct 13, 2025
71335-2799-8100 TABLET, FILM COATED in 1 BOTTLE (71335-2799-8)Oct 13, 2025
71335-2799-97 TABLET, FILM COATED in 1 BOTTLE (71335-2799-9)Oct 13, 2025

Other Atorvastatin Calcium products