"17856-0595-4" National Drug Code (NDC)

NDC Code	17856-0595-4
Package Description	1 CASE in 1 CUP, UNIT-DOSE (17856-0595-4) / 50 CUP in 1 CASE (17856-0595-3) / 30 mL in 1 CUP
Product NDC	17856-0595
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Sodium Citrate And Citric Acid
Non-Proprietary Name	Sodium Citrate And Citric Acid Monohydrate
Dosage Form	SOLUTION
Usage	ORAL
Start Marketing Date	19690101
Marketing Category Name	UNAPPROVED DRUG OTHER
Manufacturer	ATLANTIC BIOLOGICALS CORP.
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]