Home
>
National Drug Code (NDC)
>
Carbidopa and Levodopa
Carbidopa and Levodopa - 63739-046-10 - (Carbidopa and Levodopa)
Drug Information of Carbidopa and Levodopa
| Product NDC: | 63739-046 |
| Proprietary Name: | Carbidopa and Levodopa |
| Non Proprietary Name: | Carbidopa and Levodopa |
| Active Ingredient(s): | 10; 100 mg/1; mg/1 & nbsp; Carbidopa and Levodopa |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Carbidopa and Levodopa
| Product NDC: | 63739-046 |
| Labeler Name: | McKesson Packaging Services Business Unit of McKesson Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA073618 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20050121 |
Package Information of Carbidopa and Levodopa
| Package NDC: | 63739-046-10 |
| Package Description: | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-046-10) > 10 TABLET in 1 BLISTER PACK |
NDC Information of Carbidopa and Levodopa
| NDC Code | 63739-046-10 |
| Proprietary Name | Carbidopa and Levodopa |
| Package Description | 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-046-10) > 10 TABLET in 1 BLISTER PACK |
| Product NDC | 63739-046 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Carbidopa and Levodopa |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20050121 |
| Marketing Category Name | ANDA |
| Labeler Name | McKesson Packaging Services Business Unit of McKesson Corporation |
| Substance Name | CARBIDOPA; LEVODOPA |
| Strength Number | 10; 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] |
