Product NDC: | 0056-0654 |
Proprietary Name: | SINEMET |
Non Proprietary Name: | CARBIDOPA AND LEVODOPA |
Active Ingredient(s): | 25; 250 mg/1; mg/1 & nbsp; CARBIDOPA AND LEVODOPA |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0056-0654 |
Labeler Name: | Bristol-Myers Squibb Pharma Company |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA017555 |
Marketing Category: | NDA |
Start Marketing Date: | 20090601 |
Package NDC: | 0056-0654-68 |
Package Description: | 100 TABLET in 1 BOTTLE (0056-0654-68) |
NDC Code | 0056-0654-68 |
Proprietary Name | SINEMET |
Package Description | 100 TABLET in 1 BOTTLE (0056-0654-68) |
Product NDC | 0056-0654 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | CARBIDOPA AND LEVODOPA |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20090601 |
Marketing Category Name | NDA |
Labeler Name | Bristol-Myers Squibb Pharma Company |
Substance Name | CARBIDOPA; LEVODOPA |
Strength Number | 25; 250 |
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] |