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TRICITRATES

NDC 0121-0677 · PAI Holdings, LLC dba PAI Pharma

Generic namePOTASSIUM CITRATE, SODIUM CITRATE, and CITRIC ACID MONOHYDRATE
Dosage formSOLUTION
RouteORAL
Active ingredient(s)POTASSIUM CITRATE, SODIUM CITRATE, CITRIC ACID MONOHYDRATE
Strength334; 550; 500 mg/5mL; mg/5mL; mg/5mL
Pharmacologic classAcidifying Activity [MoA], Acidifying Activity [MoA], Acidifying Activity [MoA], Anti-coagulant [EPC], Anti-coagulant [EPC], Anti-coagulant [EPC], Calcium Chelating Activity [MoA], Calcium Chelating Activity [MoA], Calcium Chelating Activity [MoA], Calculi Dissolution Agent [EPC], Calculi Dissolution Agent [EPC], Calculi Dissolution Agent [EPC], Decreased Coagulation Factor Activity [PE], Decreased Coagulation Factor Activity [PE], Decreased Coagulation Factor Activity [PE]
Marketing categoryUNAPPROVED DRUG OTHER

Packages

0121-0677-16 — 473 mL in 1 BOTTLE (0121-0677-16)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0065-0795 — balanced salt solution, 0065-1795 — balanced salt solution, 0121-0595 — SODIUM CITRATE and CITRIC ACID MONOHYDRATE, 0121-0676 — Potassium Citrate and Citric Acid Monohydrate, 0121-1190 — SODIUM CITRATE and CITRIC ACID MONOHYDRATE, 0178-0610 — potassium citrate, 0178-0615 — potassium citrate, 0245-0070 — potassium citrate, 0245-0071 — potassium citrate, 0264-1945 — Sodium Chloride, Potassium Chloride, Calcium Chloride, Magnesium Chloride, Sodium Acetate, and Sodium Citrate, 0280-0047 — Anhydrous citric acid, Sodium bicarbonate (heat-treated), 0280-0079 — Anhydrous citric acid, Sodium bicarbonate (heat-treated), 0280-0083 — Anhydrous citric acid, Sodium bicarbonate (heat-treated), 0280-4100 — Alka-Seltzer Gold, 0591-2682 — Potassium Citrate, 0591-2729 — Potassium Citrate, 0591-2742 — Potassium Citrate, 14498-003 — Anticoagulant Citrate Phosphate Dextrose Solution, 14498-004 — Anticoagulant Citrate Phosphate Dextrose Solution, 14498-005 — anticoagulant citrate phosphate dextrose, +93 more

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

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels