| NDC Code | 16571-157-01 |
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| Package Description | 100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (16571-157-01) |
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| Product NDC | 16571-157 |
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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 | 20250108 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA078893 |
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| Manufacturer | Rising Pharma Holdings, Inc. |
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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 | Amino Acids, Aromatic [CS], Aromatic Amino Acid [EPC] |
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