Skip to main content

Pravastatin Sodium

NDC 35356-919 · Lake Erie Medical DBA Quality Care Products LLC

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

35356-919-30 — 30 TABLET in 1 BOTTLE (35356-919-30)

35356-919-90 — 90 TABLET in 1 BOTTLE (35356-919-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0904-5892 — PRAVASTATIN SODIUM, 0904-5893 — PRAVASTATIN SODIUM, 16714-558 — Pravastatin Sodium, 16714-559 — Pravastatin Sodium, 16714-560 — Pravastatin Sodium, 16714-570 — Pravastatin Sodium, 16729-008 — PRAVASTATIN SODIUM, 16729-009 — PRAVASTATIN SODIUM, 16729-010 — PRAVASTATIN SODIUM, 16729-011 — PRAVASTATIN SODIUM, 43063-807 — PRAVASTATIN SODIUM, 43063-808 — PRAVASTATIN SODIUM, 48433-148 — Pravastatin sodium, 48433-149 — Pravastatin sodium, 50090-0973 — Pravastatin Sodium, 50090-0975 — Pravastatin Sodium, 50090-1533 — Pravastatin Sodium, 50090-1594 — Pravastatin Sodium, 50090-2024 — PRAVASTATIN SODIUM, 50090-2025 — 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.