Potassium Chloride
- Product NDC
- 70934-741
- 11-digit product format
- 709340741
- Labeler code
- 70934
- Product ID
- 70934-741_ac9e751b-5621-16b7-e053-2995a90ac2fc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- potassium chloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. dba Northwind Pharmaceuticals
- Application
- ANDA076368
- Marketing category
- ANDA
- Marketing start
- 2020-05-26
- Marketing end
- 0000-00-00
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 20 meq/1
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 660YQ98I10 | POTASSIUM CHLORIDE | 7447-40-7 | POTASSIUM CHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-741-90 | 70934074190 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70934-741-90) | 2020-05-26 | 0000-00-00 | No | No | Current |