NDC 71335-1336 – Atorvastatin calcium

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

Human Prescription Drug

Product NDC71335-1336

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 (4)

Package NDCDescriptionSince
71335-1336-130 TABLET, FILM COATED in 1 BOTTLE (71335-1336-1)Jan 20, 2020
71335-1336-260 TABLET, FILM COATED in 1 BOTTLE (71335-1336-2)Jul 9, 2024
71335-1336-390 TABLET, FILM COATED in 1 BOTTLE (71335-1336-3)Sep 10, 2019
71335-1336-4180 TABLET, FILM COATED in 1 BOTTLE (71335-1336-4)Jul 9, 2024

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