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Pravastatin Sodium

NDC 60687-178 · American Health Packaging

FDA lists marketing as ended on 2026-08-31.
Generic namePravastatin Sodium
Dosage formTABLET
RouteORAL
Active ingredient(s)PRAVASTATIN SODIUM
Strength20 mg/1
Pharmacologic classHMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
Marketing categoryANDA

Packages

60687-178-01 — 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-178-01) / 1 TABLET in 1 BLISTER PACK (60687-178-11)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 60505-0169 — PRAVASTATIN SODIUM, 60505-0170 — PRAVASTATIN SODIUM, 60505-1323 — PRAVASTATIN SODIUM, 60687-886 — PRAVASTATIN SODIUM, 60687-897 — PRAVASTATIN SODIUM, 60687-908 — PRAVASTATIN SODIUM, 61919-708 — 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, +170 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.