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PRAVASTATIN SODIUM

NDC 68788-7009 · Preferred Pharmaceuticals 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

68788-7009-1 — 100 TABLET in 1 BOTTLE (68788-7009-1)

68788-7009-2 — 20 TABLET in 1 BOTTLE (68788-7009-2)

68788-7009-3 — 30 TABLET in 1 BOTTLE (68788-7009-3)

68788-7009-6 — 60 TABLET in 1 BOTTLE (68788-7009-6)

68788-7009-8 — 120 TABLET in 1 BOTTLE (68788-7009-8)

68788-7009-9 — 90 TABLET in 1 BOTTLE (68788-7009-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68180-485 — PRAVASTATIN SODIUM, 68180-486 — PRAVASTATIN SODIUM, 68180-487 — PRAVASTATIN SODIUM, 68180-488 — PRAVASTATIN SODIUM, 68462-195 — Pravastatin Sodium, 68462-196 — Pravastatin Sodium, 68462-197 — Pravastatin Sodium, 68462-198 — Pravastatin Sodium, 68788-4049 — Pravastatin sodium, 68788-4059 — 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, 69097-791 — PRAVASTATIN SODIUM, 69097-792 — PRAVASTATIN SODIUM, 69292-101 — 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.