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Carbidopa and Levodopa
Carbidopa and Levodopa - 76237-259-30 - (carbidopa and levodopa)
Drug Information of Carbidopa and Levodopa
| Product NDC: | 76237-259 |
| 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: | 76237-259 |
| Labeler Name: | McKesson Contract Packaging |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA075091 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120208 |
Package Information of Carbidopa and Levodopa
| Package NDC: | 76237-259-30 |
| Package Description: | 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-259-30) > 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
NDC Information of Carbidopa and Levodopa
| NDC Code | 76237-259-30 |
| Proprietary Name | Carbidopa and Levodopa |
| Package Description | 6 BLISTER PACK in 1 BOX, UNIT-DOSE (76237-259-30) > 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK |
| Product NDC | 76237-259 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | carbidopa and levodopa |
| Dosage Form Name | TABLET, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20120208 |
| Marketing Category Name | ANDA |
| Labeler Name | McKesson Contract Packaging |
| 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],Aromatic Amino Acid Decarboxylation Inhibitor [EPC],DOPA Decarboxylase Inhibitors [MoA] |
