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ATORVASTATIN CALCIUM

NDC 50228-452 · ScieGen Pharmaceuticals, Inc.

Generic nameATORVASTATIN CALCIUM
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)ATORVASTATIN CALCIUM TRIHYDRATE
Strength20 mg/1
Pharmacologic classHMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
Marketing categoryANDA

Packages

50228-452-05 — 500 TABLET, FILM COATED in 1 BOTTLE (50228-452-05)

50228-452-90 — 90 TABLET, FILM COATED in 1 BOTTLE (50228-452-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50090-7721 — atorvastatin calcium, 50090-7722 — atorvastatin calcium, 50090-7723 — atorvastatin calcium, 50090-7724 — atorvastatin calcium, 50090-7725 — atorvastatin calcium, 50090-7726 — atorvastatin calcium, 50090-7727 — atorvastatin calcium, 50090-7806 — ATORVASTATIN CALCIUM, 50090-7807 — ATORVASTATIN CALCIUM, 50228-451 — ATORVASTATIN CALCIUM, 50228-453 — ATORVASTATIN CALCIUM, 50228-454 — ATORVASTATIN CALCIUM, 51079-208 — atorvastatin calcium, 51079-209 — atorvastatin calcium, 51079-210 — atorvastatin calcium, 51079-211 — atorvastatin calcium, 51655-464 — Atorvastatin Calcium, 51655-465 — Atorvastatin Calcium, 51655-747 — Atorvastatin Calcium, 51655-946 — ATORVASTATIN CALCIUM, +365 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.