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CARBIDOPA AND LEVODOPA
CARBIDOPA AND LEVODOPA - 16729-079-01 - (Carbidopa and Levodopa)
Drug Information of CARBIDOPA AND LEVODOPA
| Product NDC: | 16729-079 |
| Proprietary Name: | CARBIDOPA AND LEVODOPA |
| Non Proprietary Name: | Carbidopa and Levodopa |
| Active Ingredient(s): | 50; 200 mg/1; mg/1 & nbsp; Carbidopa and Levodopa |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of CARBIDOPA AND LEVODOPA
| Product NDC: | 16729-079 |
| Labeler Name: | Accord Healthcare, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA202323 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20130509 |
Package Information of CARBIDOPA AND LEVODOPA
| Package NDC: | 16729-079-01 |
| Package Description: | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (16729-079-01) |
NDC Information of CARBIDOPA AND LEVODOPA
| NDC Code | 16729-079-01 |
| Proprietary Name | CARBIDOPA AND LEVODOPA |
| Package Description | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (16729-079-01) |
| Product NDC | 16729-079 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Carbidopa and Levodopa |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20130509 |
| Marketing Category Name | ANDA |
| Labeler Name | Accord Healthcare, Inc. |
| Substance Name | CARBIDOPA; LEVODOPA |
| Strength Number | 50; 200 |
| Strength Unit | mg/1; mg/1 |
| Pharmaceutical Classes | Aromatic Amino Acid Decarboxylation Inhibitor [EPC],DOPA Decarboxylase Inhibitors [MoA] |
