| NDC Code | 47335-001-88 |
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| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (47335-001-88) |
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| Product NDC | 47335-001 |
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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 | 20121002 |
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| Marketing Category Name | NDA AUTHORIZED GENERIC |
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| Application Number | NDA021485 |
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| Manufacturer | Sun Pharmaceutical Industries, Inc. |
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| Substance Name | CARBIDOPA; LEVODOPA; ENTACAPONE |
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| Strength | 12.5; 50; 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 [CS],Catechol O-Methyltransferase Inhibitors [MoA],Catechol-O-Methyltransferase Inhibitor [EPC] |
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