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Pravastatin sodium

NDC 82868-096 · Northwind Health Company, 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

82868-096-30 — 30 TABLET in 1 BOTTLE, PLASTIC (82868-096-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71610-884 — PRAVASTATIN SODIUM, 72162-1706 — PRAVASTATIN SODIUM, 72162-1951 — PRAVASTATIN SODIUM, 72162-1953 — PRAVASTATIN SODIUM, 72189-059 — PRAVASTATIN SODIUM, 72189-060 — PRAVASTATIN SODIUM, 72189-061 — PRAVASTATIN SODIUM, 72189-119 — PRAVASTATIN SODIUM, 72789-143 — PRAVASTATIN SODIUM, 72789-161 — PRAVASTATIN SODIUM, 82009-006 — PRAVASTATIN SODIUM, 82009-007 — PRAVASTATIN SODIUM, 82009-008 — PRAVASTATIN SODIUM, 82868-081 — Pravastatin sodium, 82868-091 — Pravastatin sodium, 82868-104 — PRAVASTATIN SODIUM, 84386-031 — Pravastatin sodium, 84386-032 — Pravastatin sodium, 84386-033 — Pravastatin sodium, 84386-034 — Pravastatin sodium, +170 more

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels