NDC 51662-1421 – Potassium Chloride
Potassium Chloride 149 mg/mL · Injection, Solution, Concentrate · Intravenous
Product NDC51662-1421
Product details
- Brand name
- Potassium Chloride
- Generic name
- Potassium Chloride
- Labeler
- HF Acquisition Co LLC, DBA HealthFirst
- Dosage form
- Injection, Solution, Concentrate
- Route
- Intravenous
- Marketing category
- ANDA · ANDA080205
- Marketed since
- October 18, 2019
- Listing expires
- December 31, 2026
- Pharmacologic class
- Osmotic Laxative; Potassium Salt
Active ingredients
- Potassium Chloride 149 mg/mL
Uses, dosage, side effects and warnings for Potassium Chloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 51662-1421-1 | 20 mL in 1 VIAL, SINGLE-DOSE (51662-1421-1) | Oct 18, 2019 |
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