Potassium Chloride
- Product NDC
- 68001-259
- 11-digit product format
- 680010259
- Labeler code
- 68001
- Product ID
- 68001-259_017b53b1-86e5-49ec-ab12-b15ff0c5c705
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- BluePoint Laboratories
- Application
- ANDA202128
- Marketing category
- ANDA
- Marketing start
- 2013-06-23
- Marketing end
- 0000-00-00
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 750 mg/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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68001-259-00 | 68001025900 | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68001-259-00) | 2013-06-23 | 0000-00-00 | No | No | Current |
| 68001-259-03 | 68001025903 | 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68001-259-03) | 2013-06-23 | 0000-00-00 | No | No | Current |
| 68001-259-08 | 68001025908 | 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68001-259-08) | 2013-06-23 | 0000-00-00 | No | No | Current |