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Potassium Citrate

NDC 68084-850 · American Health Packaging

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

68084-850-32 — 20 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-850-32) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (68084-850-33)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

62135-435 — Potassium Citrate and Citric Acid, 62135-438 — Tricitrates, 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, 68382-536 — Potassium Citrate, 68382-537 — 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, +44 more

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