"47335-909-18" National Drug Code (NDC)

Carbidopa, Levodopa And Entacapone 1000 TABLET, FILM COATED in 1 BOTTLE (47335-909-18)
(Sun Pharma Global FZE)

NDC Code47335-909-18
Package Description1000 TABLET, FILM COATED in 1 BOTTLE (47335-909-18)
Product NDC47335-909
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCarbidopa, Levodopa And Entacapone
Non-Proprietary NameCarbidopa, Levodopa And Entacapone
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20120522
End Marketing Date20180331
Marketing Category NameANDA
Application NumberANDA079085
ManufacturerSun Pharma Global FZE
Substance NameCARBIDOPA; LEVODOPA; ENTACAPONE
Strength25; 100; 200
Strength Unitmg/1; mg/1; mg/1
Pharmacy ClassesAromatic Amino Acid [EPC],Amino Acids, Aromatic [Chemical/Ingredient],Catechol O-Methyltransferase Inhibitors [MoA],Catechol-O-Methyltransferase Inhibitor [EPC]

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