NDC Code |
62756-187-18 |
Proprietary Name |
Carbidopa and Levodopa |
Package Description |
1000 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (62756-187-18) |
Product NDC |
62756-187 |
Product Type Name |
HUMAN PRESCRIPTION DRUG |
Non Proprietary Name |
Carbidopa and Levodopa |
Dosage Form Name |
TABLET, ORALLY DISINTEGRATING |
Route Name |
ORAL |
Start Marketing Date |
20090814 |
Marketing Category Name |
ANDA |
Labeler Name |
Sun Pharmaceutical Industries Limited |
Substance Name |
CARBIDOPA; LEVODOPA |
Strength Number |
25; 100 |
Strength Unit |
mg/1; mg/1 |
Pharmaceutical Classes |
Aromatic Amino Acid Decarboxylation Inhibitor [EPC],DOPA Decarboxylase Inhibitors [MoA],Aromatic Amino Acid Decarboxylation Inhibitor [EPC],DOPA Decarboxylase Inhibitors [MoA] |