Potassium Chloride
- Product NDC
- 68788-7748
- 11-digit product format
- 687887748
- Labeler code
- 68788
- Product ID
- 68788-7748_0d6a5877-6e0b-454f-a210-52f6e442cfa4
- 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
- 2020-07-01
- Marketing end
- 0000-00-00
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 750 mg/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 |
|---|
| 68788-7748-3 | 68788774803 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-7748-3) | 2020-07-01 | 0000-00-00 | No | No | Current |
| 68788-7748-6 | 68788774806 | 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-7748-6) | 2020-07-01 | 0000-00-00 | No | No | Current |
| 68788-7748-9 | 68788774809 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-7748-9) | 2020-07-01 | 0000-00-00 | No | No | Current |