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Potassium Citrate

NDC 62559-291 · ANI Pharmaceuticals, Inc.

Generic namePotassium Citrate
Dosage formTABLET, EXTENDED RELEASE
RouteORAL
Active ingredient(s)POTASSIUM CITRATE
Strength10 meq/1
Pharmacologic classAcidifying Activity [MoA], Anti-coagulant [EPC], Calcium Chelating Activity [MoA], Calculi Dissolution Agent [EPC], Decreased Coagulation Factor Activity [PE]
Marketing categoryANDA

Packages

62559-291-01 — 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (62559-291-01)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

42543-406 — POTASSIUM CITRATE, 42543-407 — POTASSIUM CITRATE, 42543-408 — POTASSIUM CITRATE, 44523-410 — potassium citrate, 44523-415 — potassium citrate, 51407-449 — Potassium Citrate, 51407-450 — Potassium Citrate, 51407-451 — Potassium Citrate, 62135-435 — Potassium Citrate and Citric Acid, 62135-438 — Tricitrates, 62559-292 — Potassium Citrate, 63629-1966 — Potassium Citrate, 63629-1967 — Potassium Citrate, 63629-8759 — Potassium Citrate, 65841-536 — Potassium Citrate, 65841-537 — Potassium Citrate, 65841-538 — Potassium Citrate, 68084-850 — Potassium Citrate, 68382-536 — Potassium Citrate, 68382-537 — Potassium Citrate, +44 more

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