| NDC Code | 16571-864-01 |
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| Package Description | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (16571-864-01) |
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| Product NDC | 16571-864 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Potassium Citrate |
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| Non-Proprietary Name | Potassium Citrate |
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| Dosage Form | TABLET, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20241215 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA077440 |
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| Manufacturer | Rising Pharma Holdings, Inc. |
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| Substance Name | POTASSIUM CITRATE |
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| Strength | 540 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Acidifying Activity [MoA], Anti-coagulant [EPC], Calcium Chelating Activity [MoA], Calculi Dissolution Agent [EPC], Decreased Coagulation Factor Activity [PE] |
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