| NDC Code | 47335-909-83 |
|---|
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (47335-909-83) |
|---|
| Product NDC | 47335-909 |
|---|
| 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 | 20120522 |
|---|
| End Marketing Date | 20180331 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA079085 |
|---|
| Manufacturer | Sun Pharma Global FZE |
|---|
| Substance Name | CARBIDOPA; LEVODOPA; ENTACAPONE |
|---|
| Strength | 25; 100; 200 |
|---|
| Strength Unit | mg/1; mg/1; mg/1 |
|---|
| Pharmacy Classes | Aromatic Amino Acid [EPC],Amino Acids, Aromatic [Chemical/Ingredient],Catechol O-Methyltransferase Inhibitors [MoA],Catechol-O-Methyltransferase Inhibitor [EPC] |
|---|