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PRAVASTATIN SODIUM

NDC 69097-791 · CIPLA USA INC.

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

69097-791-05 — 90 TABLET in 1 BOTTLE (69097-791-05)

69097-791-12 — 500 TABLET in 1 BOTTLE (69097-791-12)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68788-4049 — Pravastatin sodium, 68788-4059 — Pravastatin sodium, 68788-7009 — PRAVASTATIN SODIUM, 68788-7660 — PRAVASTATIN SODIUM, 68788-7779 — PRAVASTATIN SODIUM, 68788-8421 — Pravastatin Sodium, 68788-8425 — Pravastatin Sodium, 68788-8871 — Pravastatin Sodium, 69097-788 — PRAVASTATIN SODIUM, 69097-789 — PRAVASTATIN SODIUM, 69097-792 — PRAVASTATIN SODIUM, 69292-101 — Pravastatin Sodium, 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, +170 more

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