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PRAVASTATIN SODIUM

NDC 51655-976 · Northwind Health Company, LLC

Generic namePRAVASTATIN SODIUM
Dosage formTABLET
RouteORAL
Active ingredient(s)PRAVASTATIN SODIUM
Strength80 mg/1
Pharmacologic classHMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
Marketing categoryANDA

Packages

51655-976-52 — 30 TABLET in 1 BOTTLE, PLASTIC (51655-976-52)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

50268-668 — PRAVASTATIN SODIUM, 51079-458 — Pravastatin Sodium, 51079-782 — Pravastatin Sodium, 51407-887 — Pravastatin sodium, 51407-888 — Pravastatin sodium, 51407-889 — Pravastatin sodium, 51407-890 — Pravastatin sodium, 51655-343 — Pravastatin Sodium, 51655-594 — Pravastatin Sodium, 51655-708 — PRAVASTATIN SODIUM, 55111-229 — Pravastatin sodium, 55111-230 — Pravastatin sodium, 55111-231 — Pravastatin sodium, 55111-274 — Pravastatin sodium, 55154-3350 — PRAVASTATIN SODIUM, 55154-5370 — Pravastatin Sodium, 55154-7275 — PRAVASTATIN SODIUM, 55154-7998 — PRAVASTATIN SODIUM, 55700-994 — Pravastatin Sodium, 60505-0168 — 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.