NDC 42385-941 – Atorvastatin Calcium

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

Human Prescription Drug

Product NDC42385-941

Product details

Brand name
Atorvastatin Calcium
Generic name
Atorvastatin Calcium
Labeler
Laurus Labs Limited
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA214513
Marketed since
January 23, 2024
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 (6)

Package NDCDescriptionSince
42385-941-01100 TABLET, FILM COATED in 1 BOTTLE (42385-941-01)Jan 23, 2024
42385-941-05500 TABLET, FILM COATED in 1 BOTTLE (42385-941-05)Jan 23, 2024
42385-941-111000 TABLET, FILM COATED in 1 BOTTLE (42385-941-11)Jan 23, 2024
42385-941-3030 TABLET, FILM COATED in 1 BOTTLE (42385-941-30)Jan 23, 2024
42385-941-6810 BLISTER PACK in 1 CARTON (42385-941-68) / 10 TABLET, FILM COATED in 1 BLISTER PACK (42385-941-10)Jan 23, 2024
42385-941-9090 TABLET, FILM COATED in 1 BOTTLE (42385-941-90)Jan 23, 2024

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