| NDC Code | 51662-1342-1 |
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| Package Description | 10 mL in 1 VIAL, SINGLE-DOSE (51662-1342-1) |
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| Product NDC | 51662-1342 |
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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 |
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| Usage | INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS |
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| Start Marketing Date | 20181222 |
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| Marketing Category Name | NDA |
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| Application Number | NDA018803 |
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| Manufacturer | HF Acquisition Co LLC, DBA HealthFirst |
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| Substance Name | SODIUM CHLORIDE |
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| Strength | 9 |
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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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