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PRAVASTATIN SODIUM

NDC 71335-2908 · Bryant Ranch Prepack

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

71335-2908-1 — 1000 TABLET in 1 BOTTLE (71335-2908-1)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 71335-2848 — Pravastatin sodium, 71335-9692 — PRAVASTATIN SODIUM, 71610-637 — PRAVASTATIN SODIUM, 71610-877 — PRAVASTATIN SODIUM, 71610-879 — PRAVASTATIN SODIUM, 71610-884 — PRAVASTATIN SODIUM, 72162-1706 — PRAVASTATIN SODIUM, 72162-1951 — PRAVASTATIN SODIUM, 72162-1953 — PRAVASTATIN SODIUM, 72189-059 — PRAVASTATIN SODIUM, 72189-060 — 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.