Potassium chloride
- Product NDC
- 50090-7749
- 11-digit product format
- 500907749
- Labeler code
- 50090
- Product ID
- 50090-7749_5f624ab1-8eca-415e-9141-43ba1e6f7955
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA215725
- Marketing category
- ANDA
- Marketing start
- 2022-07-25
- 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
- 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 |
|---|
| 50090-7749-0 | 50090774900 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (50090-7749-0) | 2025-11-03 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Potassium chloride | A-S Medication Solutions | 2025-11-06 | HUMAN PRESCRIPTION DRUG LABEL | 1 |