Potassium Chloride
- Product NDC
- 64950-321
- 11-digit product format
- 649500321
- Labeler code
- 64950
- Product ID
- 64950-321_015c512b-8162-47af-9181-69065eef98fa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- POWDER, FOR SOLUTION
- Route
- ORAL
- Labeler
- Genus Lifesciences Inc.
- Application
- NDA208019
- Marketing category
- NDA
- Marketing start
- 2015-09-07
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 1.5 g/1.58g
- 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 | 1.5 g/1.58g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 660YQ98I10 |
| Rxcui | 1867544 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 64950-321-01 | Potassium Chloride | 100 in 1 CARTON | POWDER, FOR SOLUTION | 100 | | 4 |
| 64950-321-20 | Potassium Chloride | 1.58 g in 1 POUCH | POWDER, FOR SOLUTION | 1.58 | | 4 |
| 64950-321-30 | Potassium Chloride | 30 in 1 CARTON | POWDER, FOR SOLUTION | 30 | | 4 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| Potassium Chloride | ACTIVE INGREDIENT | 660YQ98I10 | POTASSIUM CHLORIDE POWDER, FOR SOLUTION [LEHIGH VALLEY TECHNOLOGIES, INC.] | 1 | |
| Chloride Ion | ACTIVE MOIETY | Q32ZN48698 | POTASSIUM CHLORIDE POWDER, FOR SOLUTION [LEHIGH VALLEY TECHNOLOGIES, INC.] | 1 | |
| Anhydrous Citric Acid | INACTIVE INGREDIENT | XF417D3PSL | POTASSIUM CHLORIDE POWDER, FOR SOLUTION [LEHIGH VALLEY TECHNOLOGIES, INC.] | 1 | |
| FD&C Yellow No. 6 | INACTIVE INGREDIENT | H77VEI93A8 | POTASSIUM CHLORIDE POWDER, FOR SOLUTION [LEHIGH VALLEY TECHNOLOGIES, INC.] | 1 | |
| Silicon Dioxide | INACTIVE INGREDIENT | ETJ7Z6XBU4 | POTASSIUM CHLORIDE POWDER, FOR SOLUTION [LEHIGH VALLEY TECHNOLOGIES, INC.] | 1 | |
| Sucralose | INACTIVE INGREDIENT | 96K6UQ3ZD4 | POTASSIUM CHLORIDE POWDER, FOR SOLUTION [LEHIGH VALLEY TECHNOLOGIES, INC.] | 1 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 64950-321 | POTASSIUM CHLORIDE POWDER, FOR SOLUTION [GENUS LIFESCIENCES INC.] | 4 | Current NDC, Legacy NDC, 3 package rows | 20200501_23d818e7-c076-40de-8dc1-0b51ba4be96a.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 64950-321-01 | 64950032101 | 100 POUCH in 1 CARTON (64950-321-01) / 1.58 g in 1 POUCH (64950-321-20) | 100 pouch | 2015-09-07 | 0000-00-00 | No | No | Current |
| 64950-321-20 | 64950032120 | 1.58 g in 1 POUCH | 1.58 g | | | | | Historical |
| 64950-321-30 | 64950032130 | 30 POUCH in 1 CARTON (64950-321-30) / 1.58 g in 1 POUCH (64950-321-20) | 30 pouch | 2015-09-07 | 0000-00-00 | No | No | Current |