| NDC Code | 31722-019-12 |
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| Package Description | 12 BOTTLE in 1 BOX (31722-019-12) / 120 mL in 1 BOTTLE |
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| Product NDC | 31722-019 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Diatrizoate Meglumine And Diatrizoate Sodium |
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| Non-Proprietary Name | Diatrizoate Meglumine And Diatrizoate Sodium |
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| Dosage Form | SOLUTION |
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| Usage | ORAL; RECTAL |
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| Start Marketing Date | 20231117 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA215049 |
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| Manufacturer | Camber Pharmaceuticals, Inc. |
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| Substance Name | DIATRIZOATE MEGLUMINE; DIATRIZOATE SODIUM |
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| Strength | 660; 100 |
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| Strength Unit | mg/mL; mg/mL |
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| Pharmacy Classes | Radiographic Contrast Agent [EPC], Radiographic Contrast Agent [EPC], X-Ray Contrast Activity [MoA], X-Ray Contrast Activity [MoA] |
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