| NDC Code | 70069-727-10 |
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| Package Description | 10 VIAL, PLASTIC in 1 CARTON (70069-727-10) / 50 mL in 1 VIAL, PLASTIC |
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| Product NDC | 70069-727 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Calcium Gluconate |
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| Non-Proprietary Name | Calcium Gluconate |
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| Dosage Form | INJECTION, SOLUTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20231020 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA217689 |
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| Manufacturer | Somerset Therapeutics, LLC |
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| Substance Name | CALCIUM GLUCONATE MONOHYDRATE |
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| Strength | 98 |
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| Strength Unit | mg/mL |
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| Pharmacy Classes | Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA] |
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