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PRAVASTATIN SODIUM

NDC 50090-7709 · A-S Medication Solutions

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

50090-7709-0 — 30 TABLET in 1 BOTTLE (50090-7709-0)

50090-7709-1 — 90 TABLET in 1 BOTTLE (50090-7709-1)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50090-3853 — PRAVASTATIN SODIUM, 50090-4206 — Pravastatin Sodium, 50090-5809 — Pravastatin Sodium, 50090-6826 — PRAVASTATIN SODIUM, 50090-6898 — Pravastatin Sodium, 50090-6911 — Pravastatin Sodium, 50090-7551 — Pravastatin Sodium, 50090-7552 — Pravastatin Sodium, 50090-7612 — Pravastatin sodium, 50090-7613 — Pravastatin sodium, 50090-7710 — PRAVASTATIN SODIUM, 50090-7813 — PRAVASTATIN SODIUM, 50090-7892 — Pravastatin sodium, 50090-7893 — Pravastatin sodium, 50090-7947 — Pravastatin sodium, 50090-7948 — Pravastatin sodium, 50268-665 — PRAVASTATIN SODIUM, 50268-666 — PRAVASTATIN SODIUM, 50268-667 — PRAVASTATIN SODIUM, 50268-668 — 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.