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simvastatin

NDC 51655-598 · Northwind Health Company, LLC

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

Packages

51655-598-52 — 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-598-52)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50090-7782 — Simvastatin, 50090-7783 — Simvastatin, 51407-190 — Ezetimibe and Simvastatin, 51407-191 — Ezetimibe and Simvastatin, 51407-192 — Ezetimibe and Simvastatin, 51407-193 — Ezetimibe and Simvastatin, 51655-113 — Simvastatin, 51655-387 — SIMVASTATIN, 51655-448 — Simvastatin, 51655-459 — SIMVASTATIN, 51655-643 — simvastatin, 51655-841 — Simvastatin, 53401-013 — Simvastatin, 53401-018 — Simvastatin, 53401-026 — Simvastatin, 55154-4782 — Simvastatin, 59651-835 — Ezetimibe and Simvastatin, 59651-836 — Ezetimibe and Simvastatin, 59651-837 — Ezetimibe and Simvastatin, 59651-838 — Ezetimibe and 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.