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Simvastatin

NDC 70518-3630 · REMEDYREPACK INC.

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

Packages

70518-3630-0 — 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3630-0)

70518-3630-1 — 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3630-1)

70518-3630-3 — 20 TABLET, FILM COATED in 1 BLISTER PACK (70518-3630-3)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

69367-376 — Simvastatin, 69367-377 — Simvastatin, 70377-001 — Simvastatin, 70377-002 — Simvastatin, 70377-003 — Simvastatin, 70377-004 — Simvastatin, 70377-005 — Simvastatin, 70518-0954 — SIMVASTATIN, 70518-1426 — SIMVASTATIN, 70518-3349 — SIMVASTATIN, 70518-3648 — Simvastatin, 70518-4102 — Simvastatin, 71205-192 — SIMVASTATIN, 71205-780 — Simvastatin, 71205-798 — SIMVASTATIN, 71205-809 — SIMVASTATIN, 71335-1891 — Simvastatin, 71335-1905 — Simvastatin, 71335-1906 — Simvastatin, 71335-2262 — Simvastatin, +172 more

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