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ATORVASTATIN CALCIUM

NDC 69097-897 · Cipla USA Inc.,

Generic nameATORVASTATIN CALCIUM
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)ATORVASTATIN CALCIUM TRIHYDRATE
Strength10 mg/1
Pharmacologic classHMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
Marketing categoryANDA

Packages

69097-897-05 — 90 TABLET, FILM COATED in 1 BOTTLE (69097-897-05)

69097-897-15 — 1000 TABLET, FILM COATED in 1 BOTTLE (69097-897-15)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68788-4008 — Atorvastatin calcium, 68788-4096 — Atorvastatin calcium, 68788-8094 — Atorvastatin calcium, 68788-8574 — atorvastatin calcium, 68788-8625 — atorvastatin calcium, 68788-8683 — ATORVASTATIN CALCIUM, 68788-8684 — ATORVASTATIN CALCIUM, 68788-8693 — atorvastatin calcium, film coated, 68788-8842 — atorvastatin calcium, film coated, 68788-8887 — atorvastatin calcium, film coated, 69097-898 — ATORVASTATIN CALCIUM, 69097-899 — ATORVASTATIN CALCIUM, 69097-911 — ATORVASTATIN CALCIUM, 69097-944 — ATORVASTATIN CALCIUM, 69097-945 — ATORVASTATIN CALCIUM, 69097-946 — ATORVASTATIN CALCIUM, 69097-947 — ATORVASTATIN CALCIUM, 70377-077 — atorvastatin calcium, 70377-078 — atorvastatin calcium, 70377-079 — 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.