Potassium Chloride
- Product NDC
- 68788-6772
- 11-digit product format
- 687886772
- Labeler code
- 68788
- Product ID
- 68788-6772_5ff677ee-e721-4cbb-8e39-c67fcc8334db
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- potassium chloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA076368
- Marketing category
- ANDA
- Marketing start
- 2016-10-24
- Marketing end
- 0000-00-00
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 20 meq/1
- Pharmacologic classes
- Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 68788-6772-3 | 68788677203 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-6772-3) | 2016-10-24 | 0000-00-00 | No | No | Current |
| 68788-6772-6 | 68788677206 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-6772-6) | 2016-10-24 | 0000-00-00 | No | No | Current |
| 68788-6772-9 | 68788677209 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-6772-9) | 2016-10-24 | 0000-00-00 | No | No | Current |