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Simvastatin

NDC 16714-681 · NorthStar Rx LLC

Generic nameSimvastatin
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)SIMVASTATIN
Strength5 mg/1
Pharmacologic classHMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
Marketing categoryANDA

Packages

16714-681-01 — 30 TABLET, FILM COATED in 1 BOTTLE (16714-681-01)

16714-681-02 — 90 TABLET, FILM COATED in 1 BOTTLE (16714-681-02)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0615-7992 — SIMVASTATIN, 0615-7993 — SIMVASTATIN, 0615-8056 — SIMVASTATIN, 16714-682 — Simvastatin, 16714-683 — Simvastatin, 16714-684 — Simvastatin, 16714-685 — Simvastatin, 16714-778 — ezetimibe and simvastatin, 16714-779 — ezetimibe and simvastatin, 16714-780 — ezetimibe and simvastatin, 16714-781 — ezetimibe and simvastatin, 16729-004 — simvastatin, 16729-005 — simvastatin, 16729-006 — simvastatin, 16729-007 — simvastatin, 16729-156 — simvastatin, 31722-510 — Simvastatin, 31722-511 — Simvastatin, 31722-512 — Simvastatin, 31722-513 — 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.