Skip to main content

Pravastatin sodium

NDC 65862-634 · Aurobindo Pharma Limited

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

65862-634-05 — 500 TABLET in 1 BOTTLE (65862-634-05)

65862-634-90 — 90 TABLET in 1 BOTTLE (65862-634-90)

65862-634-99 — 1000 TABLET in 1 BOTTLE (65862-634-99)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

63629-8910 — PRAVASTATIN SODIUM, 63629-8911 — PRAVASTATIN SODIUM, 63629-8912 — PRAVASTATIN SODIUM, 63629-8913 — PRAVASTATIN SODIUM, 63629-9162 — PRAVASTATIN SODIUM, 63629-9163 — PRAVASTATIN SODIUM, 63629-9164 — PRAVASTATIN SODIUM, 63629-9165 — PRAVASTATIN SODIUM, 65862-632 — Pravastatin sodium, 65862-633 — Pravastatin sodium, 65862-635 — Pravastatin sodium, 67046-1518 — PRAVASTATIN SODIUM, 67046-1519 — PRAVASTATIN SODIUM, 67046-1621 — PRAVASTATIN SODIUM, 68071-3361 — PRAVASTATIN SODIUM, 68071-3366 — PRAVASTATIN SODIUM, 68071-3788 — Pravastatin Sodium, 68071-3895 — Pravastatin sodium, 68071-5001 — PRAVASTATIN SODIUM, 68071-5007 — 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.