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Pravastatin Sodium

NDC 68462-196 · Glenmark Pharmaceuticals Inc., USA

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

68462-196-05 — 500 TABLET in 1 BOTTLE (68462-196-05)

68462-196-90 — 90 TABLET in 1 BOTTLE (68462-196-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68071-3366 — PRAVASTATIN SODIUM, 68071-3788 — Pravastatin Sodium, 68071-3895 — Pravastatin sodium, 68071-5001 — PRAVASTATIN SODIUM, 68071-5007 — PRAVASTATIN SODIUM, 68180-485 — PRAVASTATIN SODIUM, 68180-486 — PRAVASTATIN SODIUM, 68180-487 — PRAVASTATIN SODIUM, 68180-488 — PRAVASTATIN SODIUM, 68462-195 — 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, 68788-7779 — PRAVASTATIN SODIUM, 68788-8421 — Pravastatin Sodium, 68788-8425 — Pravastatin Sodium, 68788-8871 — 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.