| NDC Code | 0409-1141-02 |
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| Package Description | 25 VIAL, PHARMACY BULK PACKAGE in 1 CASE (0409-1141-02) / 100 mL in 1 VIAL, PHARMACY BULK PACKAGE (0409-1141-12) |
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| Product NDC | 0409-1141 |
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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 | 20050430 |
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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 | 234 |
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| Strength Unit | mg/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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