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PRAVASTATIN SODIUM

NDC 68180-487 · Lupin Pharmaceuticals, Inc.

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

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

67046-1519 — PRAVASTATIN SODIUM, 67046-1621 — PRAVASTATIN SODIUM, 68071-3361 — 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, 68180-488 — PRAVASTATIN SODIUM, 68462-195 — Pravastatin Sodium, 68462-196 — Pravastatin Sodium, 68462-197 — Pravastatin Sodium, 68462-198 — Pravastatin Sodium, 68788-4049 — Pravastatin sodium, 68788-4059 — Pravastatin sodium, 68788-7009 — PRAVASTATIN SODIUM, 68788-7660 — PRAVASTATIN SODIUM, 68788-7779 — 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.

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