| NDC Code | 65197-203-09 |
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| Package Description | 6 POWDER, FOR SOLUTION in 1 CARTON (65197-203-09) |
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| Product NDC | 65197-203 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Emetrol Powder |
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| Proprietary Name Suffix | Non-drowsy |
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| Non-Proprietary Name | Sodium Citrate Dihydrate |
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| Dosage Form | POWDER, FOR SOLUTION |
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| Usage | ORAL |
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| Start Marketing Date | 20231201 |
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| Marketing Category Name | UNAPPROVED DRUG OTHER |
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| Manufacturer | WellSpring Pharmaceutical Corporation |
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| Substance Name | TRISODIUM CITRATE DIHYDRATE |
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| Strength | 460 |
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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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