Potassium Chloride
- Product NDC
- 68001-235
- 11-digit product format
- 680010235
- Labeler code
- 68001
- Product ID
- 68001-235_c6eb789f-f47d-630f-e053-2a95a90aeb91
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- potassium chloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- BluePoint Laboratories
- Application
- ANDA076368
- Marketing category
- ANDA
- Marketing start
- 2014-02-25
- Marketing end
- 2022-11-30
- 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
- 0000-00-00
- 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 |
|---|
| 68001-235-00 | 68001023500 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68001-235-00) | 2014-02-25 | 0000-00-00 | No | No | Current |
| 68001-235-03 | 68001023503 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68001-235-03) | 2014-02-25 | 0000-00-00 | No | No | Current |
| 68001-235-08 | 68001023508 | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68001-235-08) | 2014-02-25 | 0000-00-00 | No | No | Current |