Potassium Chloride
- Product NDC
- 43386-917
- 11-digit product format
- 433860917
- Labeler code
- 43386
- Product ID
- 43386-917_a056d531-3e7b-4598-a042-0d498456be72
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Lupin Pharmaceuticals,Inc.
- Application
- ANDA206347
- Marketing category
- ANDA
- Marketing start
- 2016-01-21
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 20 meq/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
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| POTASSIUM CHLORIDE | 20 meq/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 660YQ98I10 |
| Rxcui | 1801294, 1801298 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 43386-917-01 | Potassium Chloride | 100 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 100 | | 3 |
| 43386-917-04 | Potassium Chloride | 400 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 400 | | 3 |
| 43386-917-05 | Potassium Chloride | 500 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 500 | | 3 |
| 43386-917-09 | Potassium Chloride | 90 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 90 | | 3 |
| 43386-917-10 | Potassium Chloride | 1000 in 1 BOTTLE | TABLET, EXTENDED RELEASE | 1000 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 43386-917 | POTASSIUM CHLORIDE TABLET, EXTENDED RELEASE [LUPIN PHARMACEUTICALS,INC.] | 3 | Current NDC, Legacy NDC, 5 package rows | 20240131_fe08221d-74d5-490a-8db4-eaf3ed20b289.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43386-917-01 | 43386091701 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (43386-917-01) | 2016-01-21 | 0000-00-00 | No | No | Current |
| 43386-917-04 | 43386091704 | 400 TABLET, EXTENDED RELEASE in 1 BOTTLE (43386-917-04) | 2016-01-21 | 0000-00-00 | No | No | Current |
| 43386-917-05 | 43386091705 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (43386-917-05) | 2017-01-30 | 0000-00-00 | No | No | Current |
| 43386-917-09 | 43386091709 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (43386-917-09) | 2016-01-21 | 0000-00-00 | No | No | Current |
| 43386-917-10 | 43386091710 | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (43386-917-10) | 2017-01-30 | 0000-00-00 | No | No | Current |