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Simvastatin

NDC 82009-014 · Quallent Pharmaceuticals Health LLC

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

82009-014-10 — 1000 TABLET, FILM COATED in 1 BOTTLE (82009-014-10)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

72865-306 — Simvastatin, 72865-307 — Simvastatin, 72865-308 — Simvastatin, 72865-309 — Simvastatin, 78206-174 — ezetimibe and simvastatin, 78206-175 — ezetimibe and simvastatin, 78206-176 — ezetimibe and simvastatin, 78206-177 — ezetimibe and simvastatin, 78206-180 — SIMVASTATIN, 78206-181 — SIMVASTATIN, 78206-182 — SIMVASTATIN, 82009-012 — Simvastatin, 82009-013 — Simvastatin, 82009-015 — Simvastatin, 82009-016 — Simvastatin, 84677-014 — Simvastatin, 84677-015 — Simvastatin, 84677-016 — Simvastatin, 84677-017 — Simvastatin, 84677-018 — 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.

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels