Sodium Chloride 51662-1464
Product NDC
51662-1464- Manufacturer
- Hf Acquisition Co Llc, Dba Healthfirst
- Dosage Form
- Injection, Solution
- Route
- Intramuscular, Intravenous, And Subcutaneous
- Product Type
- Human Prescription Drug
- Marketing Start
- December 12, 2019
- Listing Expires
- December 31, 2026
- Application
- NDA018803
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Sodium Chloride | 9 mg/mL |
Packaging Options(1)
20 mL in 1 VIAL, SINGLE-DOSE (51662-1464-1)