NDC 71335-2213 – Atorvastatin calcium

Atorvastatin 20 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-2213

Product details

Brand name
Atorvastatin calcium
Generic name
Atorvastatin calcium
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA213853
Marketed since
August 26, 2020
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
71335-2213-130 TABLET in 1 BOTTLE (71335-2213-1)Sep 6, 2023
71335-2213-260 TABLET in 1 BOTTLE (71335-2213-2)Jan 26, 2024
71335-2213-390 TABLET in 1 BOTTLE (71335-2213-3)Aug 4, 2023
71335-2213-49 TABLET in 1 BOTTLE (71335-2213-4)Jan 31, 2025
71335-2213-528 TABLET in 1 BOTTLE (71335-2213-5)Jan 31, 2025
71335-2213-620 TABLET in 1 BOTTLE (71335-2213-6)Jan 31, 2025
71335-2213-7180 TABLET in 1 BOTTLE (71335-2213-7)Oct 19, 2023
71335-2213-8100 TABLET in 1 BOTTLE (71335-2213-8)Jan 31, 2025
71335-2213-97 TABLET in 1 BOTTLE (71335-2213-9)Jan 31, 2025

Other Atorvastatin Calcium products