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PRAVASTATIN SODIUM

NDC 68788-7779 · Preferred Pharmaceuticals Inc.

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

68788-7779-3 — 90 TABLET in 1 BOTTLE (68788-7779-3)

68788-7779-6 — 100 TABLET in 1 BOTTLE (68788-7779-6)

68788-7779-9 — 500 TABLET in 1 BOTTLE (68788-7779-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 68788-7009 — PRAVASTATIN SODIUM, 68788-7660 — 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, 69292-102 — Pravastatin Sodium, 69292-103 — 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.