| NDC Code | 0713-0936-81 |
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| Package Description | 180 TABLET, FILM COATED in 1 BOTTLE (0713-0936-81) |
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| Product NDC | 0713-0936 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Colesevelam Hydrochloride |
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| Non-Proprietary Name | Colesevelam Hydrochloride |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20220801 |
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| Marketing Category Name | NDA |
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| Application Number | NDA021176 |
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| Manufacturer | Cosette Pharmaceuticals, Inc. |
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| Substance Name | COLESEVELAM HYDROCHLORIDE |
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| Strength | 625 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Bile Acid Sequestrant [EPC], Bile-acid Binding Activity [MoA] |
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