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Carbidopa and Levodopa
Carbidopa and Levodopa - 62756-187-88 - (Carbidopa and Levodopa)
Drug Information of Carbidopa and Levodopa
| Product NDC: | 62756-187 |
| Proprietary Name: | Carbidopa and Levodopa |
| Non Proprietary Name: | Carbidopa and Levodopa |
| Active Ingredient(s): | 25; 100 mg/1; mg/1 & nbsp; Carbidopa and Levodopa |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, ORALLY DISINTEGRATING |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Carbidopa and Levodopa
| Product NDC: | 62756-187 |
| Labeler Name: | Sun Pharmaceutical Industries Limited |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078690 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090814 |
Package Information of Carbidopa and Levodopa
| Package NDC: | 62756-187-88 |
| Package Description: | 100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (62756-187-88) |
NDC Information of Carbidopa and Levodopa
| NDC Code | 62756-187-88 |
| Proprietary Name | Carbidopa and Levodopa |
| Package Description | 100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (62756-187-88) |
| 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] |
