Potassium Chloride Extended-Release
- Product NDC
- 71335-2913
- 11-digit product format
- 713352913
- Labeler code
- 71335
- Product ID
- 71335-2913_cc5478c5-e0e6-4cff-830c-8a84ad2604dd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA076368
- Marketing category
- ANDA
- Marketing start
- 2019-11-20
- 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 |
|---|
| 71335-2913-1 | 71335291301 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2913-1) | 2025-11-06 | No | No | Historical |