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CARBIDOPA AND LEVODOPA
CARBIDOPA AND LEVODOPA - 62756-517-83 - (CARBIDOPA AND LEVODOPA)
Drug Information of CARBIDOPA AND LEVODOPA
| Product NDC: | 62756-517 |
| 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: | 62756-517 |
| Labeler Name: | Sun Pharmaceutical Industries Limited |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078536 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20081028 |
Package Information of CARBIDOPA AND LEVODOPA
| Package NDC: | 62756-517-83 |
| Package Description: | 30 TABLET in 1 BOTTLE (62756-517-83) |
NDC Information of CARBIDOPA AND LEVODOPA
| NDC Code | 62756-517-83 |
| Proprietary Name | CARBIDOPA AND LEVODOPA |
| Package Description | 30 TABLET in 1 BOTTLE (62756-517-83) |
| Product NDC | 62756-517 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | CARBIDOPA AND LEVODOPA |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20081028 |
| Marketing Category Name | ANDA |
| Labeler Name | Sun Pharmaceutical Industries Limited |
| 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] |
