Potassium Chloride
- Product NDC
- 68788-6771
- 11-digit product format
- 687886771
- Labeler code
- 68788
- Product ID
- 68788-6771_13d2e499-ab5d-449b-bff4-f91cf05f16cb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- NDA018279
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2016-10-24
- 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
- 2021-12-31
- 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 |
|---|
| 68788-6771-3 | 68788677103 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-6771-3) | 2016-10-24 | 0000-00-00 | No | No | Current |
| 68788-6771-6 | 68788677106 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-6771-6) | 2016-10-24 | 0000-00-00 | No | No | Current |
| 68788-6771-9 | 68788677109 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-6771-9) | 2016-10-24 | 0000-00-00 | No | No | Current |