| NDC Code | 62756-186-18 |
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| Package Description | 1000 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (62756-186-18) |
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| Product NDC | 62756-186 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Carbidopa And Levodopa |
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| Non-Proprietary Name | Carbidopa And Levodopa |
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| Dosage Form | TABLET, ORALLY DISINTEGRATING |
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| Usage | ORAL |
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| Start Marketing Date | 20090814 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA078690 |
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| Manufacturer | Sun Pharmaceutical Industries Limited |
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| Substance Name | CARBIDOPA; LEVODOPA |
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| Strength | 10; 100 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Aromatic Amino Acid Decarboxylation Inhibitor [EPC],DOPA Decarboxylase Inhibitors [MoA],Aromatic Amino Acid [EPC],Amino Acids, Aromatic [Chemical/Ingredient] |
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