0.9% Sodium Chloride 51662-1609
Product NDC
51662-1609- Manufacturer
- Hf Acquisition Co Llc, Dba Healthfirst
- Dosage Form
- Injection, Solution
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- July 31, 2022
- Listing Expires
- December 31, 2026
- Application
- ANDA207956
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Sodium Chloride | 9 g/1000mL |
Packaging Options(1)
500 mL in 1 BAG (51662-1609-1)