NDC 24979-229 – Potassium Chloride
Potassium Chloride 600 mg/1 · Tablet, Extended Release · Oral
Product NDC24979-229
Product details
- Brand name
- Potassium Chloride
- Generic name
- Potassium Chloride
- Labeler
- Upsher-Smith Laboratories, LLC
- Dosage form
- Tablet, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA218979
- Marketed since
- October 28, 2024
- Listing expires
- December 31, 2026
- Pharmacologic class
- Osmotic Laxative; Potassium Salt
Active ingredients
- Potassium Chloride 600 mg/1
Uses, dosage, side effects and warnings for Potassium Chloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 24979-229-00 | 80000 TABLET, EXTENDED RELEASE in 1 DRUM (24979-229-00) | Jun 1, 2025 |
| 24979-229-01 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (24979-229-01) | Oct 28, 2024 |
| 24979-229-03 | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (24979-229-03) | Oct 28, 2024 |
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