Potassium Chloride ER
- Product NDC
- 72189-648
- 11-digit product format
- 721890648
- Labeler code
- 72189
- Product ID
- 72189-648_44821394-e7a8-de9d-e063-6294a90a97b9
- 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
- 2025-11-04
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 750 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Potassium Chloride ER
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| POTASSIUM CHLORIDE | 750 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 660YQ98I10 |
| Rxcui | 1801298 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72189-648-04 | Potassium Chloride ER | 4 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 4 | | 2 |
| 72189-648-30 | Potassium Chloride ER | 30 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 30 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72189-648-04 | 72189064804 | 4 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-648-04) | 2025-11-04 | No | No | Current |
| 72189-648-30 | 72189064830 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-648-30) | 2025-11-04 | No | No | Current |