Skip to main content

Pravastatin Sodium

NDC 61919-708 · Direct_Rx

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

61919-708-30 — 30 TABLET in 1 BOTTLE (61919-708-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

55154-7998 — PRAVASTATIN SODIUM, 55700-994 — Pravastatin Sodium, 60505-0168 — PRAVASTATIN SODIUM, 60505-0169 — PRAVASTATIN SODIUM, 60505-0170 — PRAVASTATIN SODIUM, 60505-1323 — PRAVASTATIN SODIUM, 60687-178 — Pravastatin Sodium, 60687-886 — PRAVASTATIN SODIUM, 60687-897 — PRAVASTATIN SODIUM, 60687-908 — PRAVASTATIN SODIUM, 62135-847 — Pravastatin Sodium, 62135-848 — Pravastatin Sodium, 62135-849 — Pravastatin Sodium, 62135-850 — Pravastatin Sodium, 63629-7508 — PRAVASTATIN SODIUM, 63629-8833 — PRAVASTATIN SODIUM, 63629-8835 — PRAVASTATIN SODIUM, 63629-8836 — PRAVASTATIN SODIUM, 63629-8904 — PRAVASTATIN SODIUM, 63629-8906 — 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.