Potassium chloride
- Product NDC
- 50090-7748
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA215725
- Marketing category
- ANDA
- Substance
- POTASSIUM CHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 50090-7748-0 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7748-0) | 2025-11-03 | | No | Historical |
| 50090-7748-1 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7748-1) | 2025-11-03 | | No | Historical |
| 50090-7748-2 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7748-2) | 2025-11-03 | | No | Historical |
| 50090-7748-3 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7748-3) | 2025-11-03 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Potassium chloride | A-S Medication Solutions | 2025-11-05 | HUMAN PRESCRIPTION DRUG LABEL | 1 |