Potassium Chloride Extended-release
- Product NDC
- 71205-824
- 11-digit product format
- 712050824
- Labeler code
- 71205
- Product ID
- 71205-824_2d810852-1a61-4411-a036-0d5c41f03989
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride Extended-release
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA214452
- Marketing category
- ANDA
- Marketing start
- 2021-01-30
- 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 |
|---|
| 71205-824-03 | 71205082403 | 3 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-824-03) | 2023-08-07 | No | No | Historical |
| 71205-824-06 | 71205082406 | 6 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-824-06) | 2023-08-07 | No | No | Historical |
| 71205-824-10 | 71205082410 | 10 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-824-10) | 2023-08-07 | No | No | Historical |
| 71205-824-30 | 71205082430 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-824-30) | 2023-08-07 | No | No | Historical |
| 71205-824-60 | 71205082460 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-824-60) | 2023-08-07 | No | No | Historical |
| 71205-824-90 | 71205082490 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-824-90) | 2023-08-07 | No | No | Historical |