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POTASSIUM CITRATE

NDC 31722-129 · Camber Pharmaceuticals, Inc

Generic namePotassium Citrate
Dosage formTABLET, EXTENDED RELEASE
RouteORAL
Active ingredient(s)POTASSIUM CITRATE
Strength5 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

31722-129-01 — 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-129-01)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0121-0677 — POTASSIUM CITRATE, SODIUM CITRATE, and CITRIC ACID MONOHYDRATE, 0178-0610 — potassium citrate, 0178-0615 — potassium citrate, 0245-0070 — potassium citrate, 0245-0071 — potassium citrate, 0591-2682 — Potassium Citrate, 0591-2729 — Potassium Citrate, 0591-2742 — Potassium Citrate, 16571-864 — potassium citrate, 16571-865 — potassium citrate, 31722-130 — Potassium Citrate, 31722-132 — Potassium Citrate, 37662-2461 — Kali Citricum, 37662-2462 — Kali Citricum, 37662-2463 — Kali Citricum, 37662-2464 — Kali Citricum, 37662-2465 — Kali Citricum, 37662-2466 — Kali Citricum, 37662-2467 — Kali Citricum, 37662-2468 — Kali Citricum, +44 more

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