| NDC Code | 0781-5669-01 |
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| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (0781-5669-01) |
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| Product NDC | 0781-5669 |
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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 | 20140618 |
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| Marketing Category Name | NDA AUTHORIZED GENERIC |
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| Application Number | NDA021485 |
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| Manufacturer | Sandoz Inc |
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| Substance Name | CARBIDOPA; ENTACAPONE; LEVODOPA |
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| Strength | 50; 200; 200 |
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| Strength Unit | mg/1; mg/1; mg/1 |
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| Pharmacy Classes | Amino Acids, Aromatic [CS], Aromatic Amino Acid [EPC], Catechol O-Methyltransferase Inhibitors [MoA], Catechol-O-Methyltransferase Inhibitor [EPC] |
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