Skip to main content

Simvastatin

NDC 71335-1891 · Bryant Ranch Prepack

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

71335-1891-1 30 TABLET, FILM COATED in 1 BOTTLE (71335-1891-1)

71335-1891-2 60 TABLET, FILM COATED in 1 BOTTLE (71335-1891-2)

71335-1891-3 100 TABLET, FILM COATED in 1 BOTTLE (71335-1891-3)

71335-1891-4 90 TABLET, FILM COATED in 1 BOTTLE (71335-1891-4)

71335-1891-5 120 TABLET, FILM COATED in 1 BOTTLE (71335-1891-5)

71335-1891-6 180 TABLET, FILM COATED in 1 BOTTLE (71335-1891-6)

71335-1891-7 3 TABLET, FILM COATED in 1 BOTTLE (71335-1891-7)

71335-1891-8 10 TABLET, FILM COATED in 1 BOTTLE (71335-1891-8)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70518-0954 — SIMVASTATIN, 70518-1426 — SIMVASTATIN, 70518-3349 — SIMVASTATIN, 70518-3630 — Simvastatin, 70518-3648 — Simvastatin, 70518-4102 — Simvastatin, 71205-192 — SIMVASTATIN, 71205-780 — Simvastatin, 71205-798 — SIMVASTATIN, 71205-809 — SIMVASTATIN, 71335-1905 — Simvastatin, 71335-1906 — Simvastatin, 71335-2262 — Simvastatin, 71335-9630 — SIMVASTATIN, 71335-9636 — SIMVASTATIN, 71335-9642 — SIMVASTATIN, 71335-9717 — SIMVASTATIN, 71610-050 — simvastatin, 71610-250 — simvastatin, 71610-609 — 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.