Potassium Chloride ER
- Product NDC
- 72189-462
- 11-digit product format
- 721890462
- Labeler code
- 72189
- Product ID
- 72189-462_2c4ddf50-4e21-7c59-e063-6294a90ace41
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride ER
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA203562
- Marketing category
- ANDA
- Marketing start
- 2023-04-17
- 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
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 | 1500 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 660YQ98I10 |
| Rxcui | 1801294 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72189-462-30 | Potassium Chloride ER | 30 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 30 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72189-462 | POTASSIUM CHLORIDE ER TABLET, EXTENDED RELEASE [DIRECT_RX] | 2 | Current NDC, 1 package rows | 20250123_f988aa11-60ef-411e-e053-6294a90a522a.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72189-462-30 | 72189046230 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-462-30) | 2023-04-17 | No | No | Historical |