Skip to main content

PRAVASTATIN SODIUM

NDC 68071-3361 · NuCare 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

68071-3361-3 — 30 TABLET in 1 BOTTLE (68071-3361-3)

68071-3361-9 — 90 TABLET in 1 BOTTLE (68071-3361-9)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

63629-9163 — PRAVASTATIN SODIUM, 63629-9164 — PRAVASTATIN SODIUM, 63629-9165 — PRAVASTATIN SODIUM, 65862-632 — Pravastatin sodium, 65862-633 — Pravastatin sodium, 65862-634 — Pravastatin sodium, 65862-635 — Pravastatin sodium, 67046-1518 — PRAVASTATIN SODIUM, 67046-1519 — PRAVASTATIN SODIUM, 67046-1621 — PRAVASTATIN SODIUM, 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, +170 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.