| NDC Code | 0409-6657-25 |
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| Package Description | 25 VIAL, SINGLE-DOSE in 1 TRAY (0409-6657-25) > 20 mL in 1 VIAL, SINGLE-DOSE |
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| Product NDC | 0409-6657 |
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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 | 19840720 |
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| Marketing Category Name | NDA |
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| Application Number | NDA018897 |
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| Manufacturer | Hospira, Inc. |
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| Substance Name | SODIUM CHLORIDE |
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| Strength | 2.92 |
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| Strength Unit | g/20mL |
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| Pharmacy Classes | Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA] |
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