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POTASSIUM CITRATE

NDC 72162-2121 · Bryant Ranch Prepack

Generic namePotassium Citrate
Dosage formTABLET, EXTENDED RELEASE
RouteORAL
Active ingredient(s)POTASSIUM CITRATE
Strength15 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

72162-2121-1 — 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-2121-1)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 72162-1759 — Potassium Citrate, 72162-2120 — Potassium Citrate, 72162-2122 — Potassium Citrate, 72162-2476 — POTASSIUM CITRATE, 72162-2477 — POTASSIUM CITRATE, 72162-2478 — POTASSIUM CITRATE, 72865-191 — Potassium Citrate, 72865-192 — Potassium Citrate, 72865-193 — Potassium Citrate, 83778-002 — Teeth Whitening Kit, 83778-012 — TeethWhitening Kit, +44 more

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