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atorvastatin calcium

NDC 70710-1775 · Zydus Pharmaceuticals USA Inc.

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

Packages

70710-1775-0 — 1000 TABLET in 1 BOTTLE (70710-1775-0)

70710-1775-5 — 500 TABLET in 1 BOTTLE (70710-1775-5)

70710-1775-9 — 90 TABLET in 1 BOTTLE (70710-1775-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70518-4138 — Atorvastatin Calcium, 70518-4422 — Atorvastatin calcium, 70518-4423 — Atorvastatin calcium, 70518-4473 — Atorvastatin calcium, 70518-4474 — Atorvastatin calcium, 70518-4550 — ATORVASTATIN CALCIUM, 70518-4587 — Atorvastatin Calcium, 70518-4592 — Atorvastatin Calcium, 70710-1770 — atorvastatin calcium, 70710-1772 — atorvastatin calcium, 70710-1777 — atorvastatin calcium, 70756-247 — Atorvastatin calcium, 70756-248 — Atorvastatin calcium, 70756-249 — Atorvastatin calcium, 70756-250 — Atorvastatin calcium, 70771-1875 — atorvastatin calcium, 70771-1876 — atorvastatin calcium, 70771-1877 — atorvastatin calcium, 70771-1878 — atorvastatin calcium, 71205-098 — 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.