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PRAVASTATIN SODIUM

NDC 72189-061 · DIRECT RX

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

72189-061-30 — 30 TABLET in 1 BOTTLE (72189-061-30)

72189-061-90 — 90 TABLET in 1 BOTTLE (72189-061-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 72189-119 — PRAVASTATIN SODIUM, 72789-143 — PRAVASTATIN SODIUM, 72789-161 — PRAVASTATIN SODIUM, 82009-006 — PRAVASTATIN SODIUM, 82009-007 — PRAVASTATIN SODIUM, 82009-008 — PRAVASTATIN SODIUM, 82868-081 — Pravastatin sodium, 82868-091 — Pravastatin sodium, 82868-096 — Pravastatin sodium, 82868-104 — 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.