Potassium Chloride
- Product NDC
- 17856-1542
- 11-digit product format
- 178561542
- Labeler code
- 17856
- Product ID
- 17856-1542_24379016-c347-41f7-8752-472b7c773c2c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Atlantic Biologicals Corps
- Application
- NDA206814
- Marketing category
- NDA
- Marketing start
- 2015-05-04
- Marketing end
- 0000-00-00
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 20 meq/15mL
- Pharmacologic classes
- Potassium Compounds [CS],Potassium Salt [EPC],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 17856-1542-1 | Potassium Chloride | 15 mL in 1 CUP | SOLUTION | 15 | | 3 |
| 17856-1542-3 | Potassium Chloride | 30 mL in 1 CUP | SOLUTION | 30 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 17856-1542 | POTASSIUM CHLORIDE SOLUTION [ATLANTIC BIOLOGICALS CORPS] | 3 | Legacy NDC, 2 package rows | 20190921_7b93a467-e0e7-40c4-8709-24b6071043e0.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 17856-1542-1 | 17856154201 | 15 mL in 1 CUP | 15 ml | Historical |
| 17856-1542-3 | 17856154203 | 30 mL in 1 CUP | 30 ml | Historical |