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Simvastatin

NDC 69367-374 · Westminster Pharmaceuticals, 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

69367-374-09 — 90 TABLET, FILM COATED in 1 BOTTLE (69367-374-09)

69367-374-10 — 1000 TABLET, FILM COATED in 1 BOTTLE (69367-374-10)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68462-322 — ezetimibe and simvastatin, 68462-323 — ezetimibe and simvastatin, 68462-324 — ezetimibe and simvastatin, 68788-8342 — SIMVASTATIN, 68788-8369 — SIMVASTATIN, 68788-8406 — SIMVASTATIN, 69238-1155 — Ezetimibe and Simvastatin, 69238-1156 — Ezetimibe and Simvastatin, 69238-1157 — Ezetimibe and Simvastatin, 69238-1158 — Ezetimibe and Simvastatin, 69367-375 — Simvastatin, 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, +172 more

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