NDC 68999-438 – Tricitrates

Potassium Citrate 550 mg/5mL; Sodium Citrate 500 mg/5mL; Citric Acid Monohydrate 334 mg/5mL · Solution · Oral

Human Prescription Drug

Product NDC68999-438

Product details

Brand name
Tricitrates
Generic name
Tricitrates
Labeler
Chartwell Governmental & Specialty RX, LLC.
Dosage form
Solution
Route
Oral
Marketing category
UNAPPROVED DRUG OTHER
Marketed since
December 8, 2022
Listing expires
December 31, 2027
Pharmacologic class
Anti-coagulant; Anti-coagulant; Anti-coagulant; Calculi Dissolution Agent; Calculi Dissolution Agent; Calculi Dissolution Agent

Active ingredients

Uses, dosage, side effects and warnings for Tricitrates →

Package NDC codes (1)

Package NDCDescriptionSince
68999-438-242 TRAY in 1 BOX (68999-438-24) / 10 CUP in 1 TRAY / 5 mL in 1 CUP (68999-438-05)Feb 20, 2026

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