Skip to main content

Pravastatin Sodium

NDC 70518-2887 · REMEDYREPACK INC.

FDA lists marketing as ended on 2026-08-31.
Generic namePravastatin Sodium
Dosage formTABLET
RouteORAL
Active ingredient(s)PRAVASTATIN SODIUM
Strength20 mg/1
Pharmacologic classHMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
Marketing categoryANDA

Packages

70518-2887-1 — 90 TABLET in 1 BOTTLE, PLASTIC (70518-2887-1)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

69292-102 — Pravastatin Sodium, 69292-103 — Pravastatin Sodium, 69292-104 — Pravastatin Sodium, 70377-045 — Pravastatin sodium, 70377-046 — Pravastatin sodium, 70377-047 — Pravastatin sodium, 70377-048 — Pravastatin sodium, 70518-0549 — PRAVASTATIN SODIUM, 70518-0876 — PRAVASTATIN SODIUM, 70518-1938 — PRAVASTATIN SODIUM, 70518-4339 — Pravastatin sodium, 70518-4408 — Pravastatin sodium, 71205-121 — PRAVASTATIN SODIUM, 71205-149 — PRAVASTATIN SODIUM, 71205-294 — Pravastatin Sodium, 71205-516 — PRAVASTATIN SODIUM, 71335-0296 — PRAVASTATIN SODIUM, 71335-0692 — PRAVASTATIN SODIUM, 71335-0947 — PRAVASTATIN SODIUM, 71335-1022 — PRAVASTATIN SODIUM, +170 more

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