"23359-016-16" National Drug Code (NDC)

NDC Code	23359-016-16
Package Description	473 mL in 1 BOTTLE (23359-016-16)
Product NDC	23359-016
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Lexuss 210
Non-Proprietary Name	Codeine Phosphate And Chlorpheniramine Maleate
Dosage Form	LIQUID
Usage	ORAL
Start Marketing Date	20090415
Marketing Category Name	UNAPPROVED DRUG OTHER
Manufacturer	Centurion Labs
Substance Name	CODEINE PHOSPHATE; CHLORPHENIRAMINE MALEATE
Strength	10; 2
Strength Unit	mg/5mL; mg/5mL
Pharmacy Classes	Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC]
DEA Schedule	CV