"0056-0521-85" National Drug Code (NDC)

NDC Code	0056-0521-85
Package Description	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (0056-0521-85)
Product NDC	0056-0521
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Sinemet
Proprietary Name Suffix	Cr
Non-Proprietary Name	Carbidopa And Levodopa
Dosage Form	TABLET, EXTENDED RELEASE
Usage	ORAL
Start Marketing Date	20090601
End Marketing Date	20140622
Marketing Category Name	NDA
Application Number	NDA019856
Manufacturer	Bristol-Myers Squibb Pharma Company
Substance Name	CARBIDOPA; LEVODOPA
Strength	50; 200
Strength Unit	mg/1; mg/1
Pharmacy Classes	Aromatic Amino Acid Decarboxylation Inhibitor [EPC],DOPA Decarboxylase Inhibitors [MoA],Aromatic Amino Acid Decarboxylation Inhibitor [EPC],DOPA Decarboxylase Inhibitors [MoA]