Potassium Chloride
- Product NDC
- 17856-1543
- 11-digit product format
- 178561543
- Labeler code
- 17856
- Product ID
- 17856-1543_b0d32d53-e93a-466f-9a74-d29a45e1d687
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- ATLANTIC BIOLOGICALS CORP.
- Application
- NDA206814
- Marketing category
- NDA
- Marketing start
- 2017-02-01
- 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 |
|---|
| 17856-1543-1 | Potassium Chloride | 15 mL in 1 CUP, UNIT-DOSE | SOLUTION | 15 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 17856-1543 | POTASSIUM CHLORIDE SOLUTION [ATLANTIC BIOLOGICALS CORP.] | 3 | Legacy NDC, 1 package rows | 20190921_509247a3-1a68-4a36-897d-0c3ade569339.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 17856-1543-1 | 17856154301 | 15 mL in 1 CUP, UNIT-DOSE | 15 ml | Historical |