Potassium Chloride
- Product NDC
- 17856-1544
- 11-digit product format
- 178561544
- Labeler code
- 17856
- Product ID
- 17856-1544_402b016e-342c-4162-9ce8-f129aa1b9f52
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- ATLANTIC BIOLOGICALS CORP.
- Application
- NDA206814
- Marketing category
- NDA
- Marketing start
- 2015-05-04
- Marketing end
- 0000-00-00
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 40 meq/15mL
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 17856-1544-1 | Potassium Chloride | 72 in 1 BOX, UNIT-DOSE | SOLUTION | 72 | | 3 |
| 17856-1544-2 | Potassium Chloride | 15 mL in 1 CUP | SOLUTION | 15 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 17856-1544 | POTASSIUM CHLORIDE SOLUTION [ATLANTIC BIOLOGICALS CORP.] | 3 | Legacy NDC, 2 package rows | 20240606_cc912caf-f4d9-4c08-ba9f-45c5e8ed8060.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 |
|---|
| 17856-1544-1 | 17856154401 | 72 CUP in 1 BOX, UNIT-DOSE (17856-1544-1) > 15 mL in 1 CUP (17856-1544-2) | 72 cup | 2022-09-22 | 0000-00-00 | No | No | Current |
| 17856-1544-2 | 17856154402 | 15 mL in 1 CUP | 15 ml | | | | | Historical |