| NDC Code | 63323-090-40 |
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| Package Description | 25 VIAL, PLASTIC in 1 TRAY (63323-090-40) > 40 mL in 1 VIAL, PLASTIC (63323-090-04) |
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| Product NDC | 63323-090 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Sodium Chloride |
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| Non-Proprietary Name | Sodium Chloride |
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| Dosage Form | INJECTION, SOLUTION, CONCENTRATE |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20210428 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA212070 |
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| Manufacturer | Fresenius Kabi USA, LLC |
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| Substance Name | SODIUM CHLORIDE |
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| Strength | 2.5 |
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| Strength Unit | meq/mL |
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| Pharmacy Classes | Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC] |
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