| NDC Code | 68462-620-30 |
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| Package Description | 30 PACKET in 1 BOX (68462-620-30) / 1 POWDER, FOR SUSPENSION in 1 PACKET |
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| Product NDC | 68462-620 |
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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 | POWDER, FOR SUSPENSION |
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| Usage | ORAL |
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| Start Marketing Date | 20180716 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA202190 |
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| Manufacturer | Glenmark Pharmaceuticals Inc.,USA |
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| Substance Name | COLESEVELAM HYDROCHLORIDE |
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| Strength | 3.75 |
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| Strength Unit | g/1 |
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| Pharmacy Classes | Bile Acid Sequestrant [EPC], Bile-acid Binding Activity [MoA] |
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