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Pravastatin Sodium

NDC 16714-560 · NorthStar RxLLC

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

16714-560-01 — 90 TABLET in 1 BOTTLE (16714-560-01)

16714-560-02 — 500 TABLET in 1 BOTTLE (16714-560-02)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0615-8542 — PRAVASTATIN SODIUM, 0615-8618 — PRAVASTATIN SODIUM, 0615-8619 — PRAVASTATIN SODIUM, 0615-8620 — PRAVASTATIN SODIUM, 0615-8621 — PRAVASTATIN SODIUM, 0904-5891 — PRAVASTATIN SODIUM, 0904-5892 — PRAVASTATIN SODIUM, 0904-5893 — PRAVASTATIN SODIUM, 16714-558 — Pravastatin Sodium, 16714-559 — 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, 48433-149 — 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.