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Tricitrates

NDC 62135-438 · Chartwell RX, LLC

Generic nameTricitrates
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

62135-438-24 — 2 TRAY in 1 BOX (62135-438-24) / 10 CUP in 1 TRAY / 5 mL in 1 CUP (62135-438-05)

62135-438-47 — 473 mL in 1 BOTTLE (62135-438-47)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

46287-014 — Citric Acid and Sodium Citrate, 47682-135 — aspirin, citric acid, sodium bicarbonate, 50268-182 — SODIUM CITRATE and CITRIC ACID MONOHYDRATE, 50268-183 — SODIUM CITRATE and CITRIC ACID MONOHYDRATE, 50402-100 — citric acid anhydrous and 13C urea, 51407-449 — Potassium Citrate, 51407-450 — Potassium Citrate, 51407-451 — Potassium Citrate, 62135-434 — Sodium Citrate and Citric Acid, 62135-435 — Potassium Citrate and Citric Acid, 62135-868 — Sodium Citrate and Citric Acid, 62135-869 — Sodium Citrate and Citric Acid, 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, +93 more

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