Potassium Chloride 51662-1421
Product NDC
51662-1421- Manufacturer
- Hf Acquisition Co Llc, Dba Healthfirst
- Dosage Form
- Injection, Solution, Concentrate
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- October 18, 2019
- Listing Expires
- December 31, 2026
- Application
- ANDA080205
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Potassium Chloride | 149 mg/mL |
Drug Class
Increased Large Intestinal Motility [PE]Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]Osmotic Activity [MoA]
Packaging Options(1)
20 mL in 1 VIAL, SINGLE-DOSE (51662-1421-1)