NDC Code | 64679-782-02 |
Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (64679-782-02) |
Product NDC | 64679-782 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Carbidopa, Levodopa And Entacapone |
Non-Proprietary Name | Carbidopa, Levodopa And Entacapone |
Dosage Form | TABLET, FILM COATED |
Usage | ORAL |
Start Marketing Date | 20120229 |
Marketing Category Name | NDA AUTHORIZED GENERIC |
Application Number | NDA021485 |
Manufacturer | Wockhardt USA LLC. |
Substance Name | LEVODOPA; ENTACAPONE; CARBIDOPA |
Strength | 50; 200; 12.5 |
Strength Unit | mg/1; mg/1; mg/1 |
Pharmacy Classes | Aromatic Amino Acid Decarboxylation Inhibitor [EPC],DOPA Decarboxylase Inhibitors [MoA],Catechol O-Methyltransferase Inhibitors [MoA],Catechol-O-Methyltransferase Inhibitor [EPC] |