NDC 42806-422 – Potassium Chloride
Potassium Chloride 600 mg/1 · Tablet, Film Coated, Extended Release · Oral
Product NDC42806-422
Product details
- Brand name
- Potassium Chloride
- Generic name
- Potassium Chloride
- Labeler
- Epic Pharma, LLC
- Dosage form
- Tablet, Film Coated, Extended Release
- Route
- Oral
- Marketing category
- ANDA · ANDA209314
- Marketed since
- August 7, 2023
- 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 |
|---|---|---|
| 42806-422-01 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42806-422-01) | Aug 7, 2023 |
| 42806-422-05 | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42806-422-05) | Aug 7, 2023 |
| 42806-422-10 | 1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42806-422-10) | Aug 7, 2023 |
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