NDC 70377-080 – Atorvastatin Calcium

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

Human Prescription Drug 1 recall

Product NDC70377-080

Product details

Brand name
Atorvastatin Calcium
Generic name
Atorvastatin calcium
Labeler
Biocon Pharma Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA216436
Marketed since
March 1, 2023
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 (3)

Package NDCDescriptionSince
70377-080-1190 TABLET, FILM COATED in 1 BOTTLE (70377-080-11)Mar 1, 2023
70377-080-12500 TABLET, FILM COATED in 1 BOTTLE (70377-080-12)Mar 1, 2023
70377-080-131000 TABLET, FILM COATED in 1 BOTTLE (70377-080-13)Mar 1, 2023

Recalls mentioning this NDC

Other Atorvastatin Calcium products