| NDC Code | 68462-433-18 |
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| Package Description | 180 TABLET, FILM COATED in 1 BOTTLE (68462-433-18) |
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| Product NDC | 68462-433 |
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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 | 20180518 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA203480 |
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| Manufacturer | Glenmark Pharmaceuticals Inc., USA |
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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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