Potassium chloride
- Product NDC
- 31722-494
- 11-digit product format
- 317220494
- Labeler code
- 31722
- Product ID
- 31722-494_7162658b-9e13-487e-bcf1-eda778fa3ac0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- potassium chloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Camber Pharmaceuticals, Inc.
- Application
- ANDA211992
- Marketing category
- ANDA
- Marketing start
- 2024-12-26
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 20 meq/15mL
- 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 | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 31722-494-47 | 31722049447 | 473 mL in 1 BOTTLE, PLASTIC (31722-494-47) | 473 ml | 2024-12-26 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Potassium chloride | Camber Pharmaceuticals, Inc. | Ascent Pharmaceuticals, Inc. | 2025-07-17 | HUMAN PRESCRIPTION DRUG LABEL | 1 |