"81033-017-50" National Drug Code (NDC)

NDC Code	81033-017-50
Package Description	100 CUP, UNIT-DOSE in 1 CASE (81033-017-50) / 15 mL in 1 CUP, UNIT-DOSE (81033-017-15)
Product NDC	81033-017
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Sodium Citrate And Citric Acid
Non-Proprietary Name	Sodium Citrate And Citric Acid
Dosage Form	SOLUTION
Usage	ORAL
Start Marketing Date	20250401
Marketing Category Name	UNAPPROVED DRUG OTHER
Manufacturer	Kesin Pharma Corporation
Substance Name	ANHYDROUS CITRIC ACID; SODIUM CITRATE
Strength	334; 500
Strength Unit	mg/5mL; mg/5mL
Pharmacy Classes	Acidifying Activity [MoA], Acidifying Activity [MoA], Anti-coagulant [EPC], Anti-coagulant [EPC], Calcium Chelating Activity [MoA], Calcium Chelating Activity [MoA], Calculi Dissolution Agent [EPC], Calculi Dissolution Agent [EPC], Decreased Coagulation Factor Activity [PE], Decreased Coagulation Factor Activity [PE]