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Atorvastatin calcium

NDC 70756-250 · Lifestar Pharma LLC

Generic nameAtorvastatin calcium
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)ATORVASTATIN CALCIUM TRIHYDRATE
Strength80 mg/1
Pharmacologic classHMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
Marketing categoryANDA

Packages

70756-250-30 — 30 TABLET, FILM COATED in 1 BOTTLE (70756-250-30)

70756-250-51 — 500 TABLET, FILM COATED in 1 BOTTLE (70756-250-51)

70756-250-90 — 90 TABLET, FILM COATED in 1 BOTTLE (70756-250-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70518-4550 — ATORVASTATIN CALCIUM, 70518-4587 — Atorvastatin Calcium, 70518-4592 — Atorvastatin Calcium, 70710-1770 — atorvastatin calcium, 70710-1772 — atorvastatin calcium, 70710-1775 — atorvastatin calcium, 70710-1777 — atorvastatin calcium, 70756-247 — Atorvastatin calcium, 70756-248 — Atorvastatin calcium, 70756-249 — Atorvastatin calcium, 70771-1875 — atorvastatin calcium, 70771-1876 — atorvastatin calcium, 70771-1877 — atorvastatin calcium, 70771-1878 — atorvastatin calcium, 71205-098 — Atorvastatin Calcium, 71205-246 — ATORVASTATIN CALCIUM, 71205-247 — ATORVASTATIN CALCIUM, 71205-264 — Atorvastatin Calcium, 71205-335 — Atorvastatin calcium, 71205-731 — 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.