0.9% Sodium Chloride 51662-1359
Product NDC
51662-1359- Manufacturer
- Hf Acquisition Co Llc, Dba Healthfirst
- Dosage Form
- Injection, Solution
- Route
- Intramuscular, Intravenous, And Subcutaneous
- Product Type
- Human Prescription Drug
- Marketing Start
- July 18, 2019
- Listing Expires
- December 31, 2026
- Application
- NDA018803
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Sodium Chloride | 9 mg/mL |
Drug Class
Increased Large Intestinal Motility [PE]Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]Osmotic Activity [MoA]
Packaging Options(1)
50 mL in 1 VIAL, PLASTIC (51662-1359-1)