| NDC Code: |
47335-909 |
| Proprietary Name: |
Carbidopa, Levodopa and Entacapone |
| Suffix: |
|
| Non-Proprietary Name: |
Carbidopa, Levodopa and Entacapone |
| Dosage Form: |
TABLET, FILM COATED |
| Method: |
ORAL |
| Original Marketing Date: |
22-05-2012 |
| Category Name: |
ANDA |
| Application Number: |
ANDA079085 |
| Labeler: |
SUN PHARMA GLOBAL FZE |
| Substance Name: |
CARBIDOPA; ENTACAPONE; LEVODOPA |
| Active Numerator Strength: |
25; 200; 100 |
| Active Ingredient Unit: |
mg/1; mg/1; mg/1 |
| Pharm Classes: |
Aromatic Amino Acid Decarboxylation Inhibitor [EPC],DOPA Decarboxylase Inhibitors [MoA],Aromatic Amino Acid Decarboxylation Inhibitor [EPC],DOPA Decarboxylase Inhibitors [MoA],Catechol O-Methyltransferase Inhibitors [MoA],Catechol-O-Methyltransferase Inhibitor [EPC] |
| DEA Schedule: |
|
