"62135-438-47" National Drug Code (NDC)

NDC Code	62135-438-47
Package Description	473 mL in 1 BOTTLE (62135-438-47)
Product NDC	62135-438
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Tricitrates
Non-Proprietary Name	Tricitrates
Dosage Form	SOLUTION
Usage	ORAL
Start Marketing Date	20221208
Marketing Category Name	UNAPPROVED DRUG OTHER
Manufacturer	Chartwell RX, LLC
Substance Name	CITRIC ACID MONOHYDRATE; POTASSIUM CITRATE; SODIUM CITRATE
Strength	334; 550; 500
Strength Unit	mg/5mL; mg/5mL; mg/5mL
Pharmacy Classes	Acidifying 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]