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"0115-3922-02" National Drug Code (NDC)

Carbidopa And Levodopa 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (0115-3922-02)
(Global Pharmaceuticals, Division of Impax Laboratories Inc.)

NDC Code0115-3922-02
Package Description500 TABLET, EXTENDED RELEASE in 1 BOTTLE (0115-3922-02)
Product NDC0115-3922
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameCarbidopa And Levodopa
Non-Proprietary NameCarbidopa And Levodopa
Dosage FormTABLET, EXTENDED RELEASE
UsageORAL
Start Marketing Date20040514
Marketing Category NameANDA
Application NumberANDA076521
ManufacturerGlobal Pharmaceuticals, Division of Impax Laboratories Inc.
Substance NameCARBIDOPA; LEVODOPA
Strength25; 100
Strength Unitmg/1; mg/1
Pharmacy ClassesAromatic Amino Acid Decarboxylation Inhibitor [EPC],DOPA Decarboxylase Inhibitors [MoA],Aromatic Amino Acid Decarboxylation Inhibitor [EPC],DOPA Decarboxylase Inhibitors [MoA]

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