Potassium Chloride ER
- Product NDC
- 72189-629
- 11-digit product format
- 721890629
- Labeler code
- 72189
- Product ID
- 72189-629_377854ff-8035-c7ac-e063-6294a90a0817
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride ER
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA214452
- Marketing category
- ANDA
- Marketing start
- 2025-06-13
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 1500 mg/1
- Pharmacologic classes
- Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 660YQ98I10 | POTASSIUM CHLORIDE | 7447-40-7 | POTASSIUM CHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72189-629-30 | 72189062930 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-629-30) | 2025-06-13 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Potassium Chloride ER | Direct_Rx | 2025-06-13 | HUMAN PRESCRIPTION DRUG LABEL | 1 |