Potassium Chloride Extended-release
- Product NDC
- 82804-109
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride Extended-release
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA214452
- Marketing category
- ANDA
- Substance
- POTASSIUM CHLORIDE
- Current FDA listing
- Yes
Related Records
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|---|---|---|---|---|
| 82804-109-30 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (82804-109-30) | 2024-06-14 | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|---|---|---|---|
| Potassium Chloride Extended-Release Tablets USP, 10 mEq Rx only | Proficient Rx LP | 2024-06-01 | HUMAN PRESCRIPTION DRUG LABEL | 1 |