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Atorvastatin calcium

NDC 70518-3783 · REMEDYREPACK INC.

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

Packages

70518-3783-1 — 90 TABLET in 1 BOTTLE, PLASTIC (70518-3783-1)

70518-3783-2 — 30 TABLET in 1 BOTTLE, PLASTIC (70518-3783-2)

70518-3783-3 — 100 TABLET in 1 BOTTLE, PLASTIC (70518-3783-3)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

60290-039 — Atorvastatin calcium, 60290-040 — Atorvastatin calcium, 60290-041 — Atorvastatin calcium, 60290-042 — Atorvastatin calcium, 68071-2967 — Atorvastatin calcium, 70518-3848 — Atorvastatin calcium, 70518-4321 — Atorvastatin calcium, 71335-2213 — Atorvastatin calcium, 71335-2697 — Atorvastatin calcium, 71335-9646 — Atorvastatin calcium, 72189-291 — ATORVASTATIN CALCIUM, 72189-531 — Atorvastatin Calcium, 75834-255 — Atorvastatin calcium, 75834-256 — Atorvastatin calcium, 75834-257 — Atorvastatin calcium, 75834-258 — Atorvastatin calcium, 82804-056 — Atorvastatin calcium

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