Potassium Chloride
- Product NDC
- 82804-075
- 11-digit product format
- 828040075
- Labeler code
- 82804
- Product ID
- 82804-075_61daa681-05a0-4b2f-a6d0-c6fc1044f521
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA075604
- Marketing category
- ANDA
- Marketing start
- 2002-04-10
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 20 meq/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 |
|---|
| 82804-075-03 | 82804007503 | 3 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-075-03) | 2024-02-12 | No | No | Historical |
| 82804-075-06 | 82804007506 | 6 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-075-06) | 2024-02-12 | No | No | Historical |
| 82804-075-10 | 82804007510 | 10 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-075-10) | 2024-02-12 | No | No | Historical |
| 82804-075-30 | 82804007530 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-075-30) | 2024-02-12 | No | No | Historical |
| 82804-075-60 | 82804007560 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-075-60) | 2024-02-12 | No | No | Historical |
| 82804-075-90 | 82804007590 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (82804-075-90) | 2024-02-12 | No | No | Historical |