Sodium Chloride 51662-1522
Product NDC
51662-1522- Manufacturer
- Hf Acquisition Co Llc, Dba Healthfirst
- Dosage Form
- Injection, Solution
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- August 4, 2020
- Listing Expires
- December 31, 2026
- Application
- NDA016366
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Sodium Chloride | 900 mg/100mL |
Packaging Options(1)
500 mL in 1 BAG (51662-1522-1)