Potassium Chloride
- Product NDC
- 50090-6867
- 11-digit product format
- 500906867
- Labeler code
- 50090
- Product ID
- 50090-6867_6a6563cf-3112-4560-ab33-63ac5b41783e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- potassium chloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA074726
- Marketing category
- ANDA
- Marketing start
- 1998-11-20
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 1500 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
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 660YQ98I10 | POTASSIUM CHLORIDE | 7447-40-7 | POTASSIUM CHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-6867-0 | 50090686700 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (50090-6867-0) | 2023-12-04 | No | No | Historical |