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Pravastatin sodium

NDC 48433-149 · Safecor Health LLC

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

48433-149-20 — 100 BLISTER PACK in 1 CARTON (48433-149-20) / 1 TABLET in 1 BLISTER PACK (48433-149-01)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

16714-560 — Pravastatin Sodium, 16714-570 — Pravastatin Sodium, 16729-008 — PRAVASTATIN SODIUM, 16729-009 — PRAVASTATIN SODIUM, 16729-010 — PRAVASTATIN SODIUM, 16729-011 — PRAVASTATIN SODIUM, 35356-919 — pravastatin sodium, 43063-807 — PRAVASTATIN SODIUM, 43063-808 — PRAVASTATIN SODIUM, 48433-148 — 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, 50090-3204 — PRAVASTATIN SODIUM, 50090-3853 — PRAVASTATIN SODIUM, 50090-4206 — Pravastatin Sodium, 50090-5809 — 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.