Potassium Chloride
- Product NDC
- 82804-057
- 11-digit product format
- 828040057
- Labeler code
- 82804
- Product ID
- 82804-057_d0ce0bdf-5f24-4093-813f-881c61d7fcc7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA209688
- Marketing category
- ANDA
- Marketing start
- 2023-04-10
- 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 |
|---|
| 82804-057-30 | 82804005730 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-057-30) | 2024-01-15 | No | No | Historical |
| 82804-057-60 | 82804005760 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-057-60) | 2024-01-15 | No | No | Historical |
| 82804-057-90 | 82804005790 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-057-90) | 2024-01-15 | No | No | Historical |