NDC 0121-0677 – Tricitrates

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

Human Prescription Drug

Product NDC0121-0677

Product details

Brand name
Tricitrates
Generic name
POTASSIUM CITRATE, SODIUM CITRATE, and CITRIC ACID MONOHYDRATE
Labeler
PAI Holdings, LLC dba PAI Pharma
Dosage form
Solution
Route
Oral
Marketing category
UNAPPROVED DRUG OTHER
Marketed since
May 25, 2005
Listing expires
December 31, 2026
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
0121-0677-16473 mL in 1 BOTTLE (0121-0677-16)May 25, 2005

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