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PRAVASTATIN SODIUM

NDC 71205-516 · Proficient Rx LP

Generic namePRAVASTATIN SODIUM
Dosage formTABLET
RouteORAL
Active ingredient(s)PRAVASTATIN SODIUM
Strength40 mg/1
Pharmacologic classHMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
Marketing categoryANDA

Packages

71205-516-30 — 30 TABLET in 1 BOTTLE (71205-516-30)

71205-516-60 — 60 TABLET in 1 BOTTLE (71205-516-60)

71205-516-90 — 90 TABLET in 1 BOTTLE (71205-516-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

70377-048 — Pravastatin sodium, 70518-0549 — PRAVASTATIN SODIUM, 70518-0876 — PRAVASTATIN SODIUM, 70518-1938 — PRAVASTATIN SODIUM, 70518-2887 — Pravastatin Sodium, 70518-4339 — Pravastatin sodium, 70518-4408 — Pravastatin sodium, 71205-121 — PRAVASTATIN SODIUM, 71205-149 — PRAVASTATIN SODIUM, 71205-294 — Pravastatin Sodium, 71335-0296 — PRAVASTATIN SODIUM, 71335-0692 — PRAVASTATIN SODIUM, 71335-0947 — PRAVASTATIN SODIUM, 71335-1022 — PRAVASTATIN SODIUM, 71335-1243 — PRAVASTATIN SODIUM, 71335-2253 — PRAVASTATIN SODIUM, 71335-2298 — PRAVASTATIN SODIUM, 71335-2687 — Pravastatin sodium, 71335-2746 — Pravastatin sodium, 71335-2833 — 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.