| NDC Code | 47335-909-18 |
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| Package Description | 1000 TABLET, FILM COATED in 1 BOTTLE (47335-909-18) |
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| Product NDC | 47335-909 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Carbidopa, Levodopa And Entacapone |
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| Non-Proprietary Name | Carbidopa, Levodopa And Entacapone |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20120522 |
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| End Marketing Date | 20180331 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA079085 |
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| Manufacturer | Sun Pharma Global FZE |
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| Substance Name | CARBIDOPA; LEVODOPA; ENTACAPONE |
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| Strength | 25; 100; 200 |
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| Strength Unit | mg/1; mg/1; mg/1 |
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| Pharmacy Classes | Aromatic Amino Acid [EPC],Amino Acids, Aromatic [Chemical/Ingredient],Catechol O-Methyltransferase Inhibitors [MoA],Catechol-O-Methyltransferase Inhibitor [EPC] |
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