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Potassium Citrate

NDC 68382-537 · Zydus Pharmaceuticals (USA) 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

68382-537-01 — 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-537-01)

68382-537-05 — 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-537-05)

68382-537-06 — 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-537-06)

68382-537-10 — 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-537-10)

68382-537-16 — 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-537-16)

68382-537-30 — 10 BLISTER PACK in 1 CARTON (68382-537-30) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

62559-291 — Potassium Citrate, 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, 68382-538 — Potassium Citrate, 68999-435 — Potassium Citrate and Citric Acid, 68999-438 — Tricitrates, 70518-3160 — Potassium Citrate, 70518-4477 — Potassium Citrate, 71335-1706 — POTASSIUM CITRATE, 71335-1967 — Potassium Citrate, 71335-2871 — POTASSIUM CITRATE, 71335-2897 — Potassium Citrate, 72162-1758 — 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.