Potassium Chloride Extended-release
- Product NDC
- 71335-2503
- 11-digit product format
- 713352503
- Labeler code
- 71335
- Product ID
- 71335-2503_541c34f6-fee2-4878-ac6c-5a46ac3be59d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride Extended-release
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA214452
- Marketing category
- ANDA
- Marketing start
- 2021-01-30
- 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 |
|---|
| 71335-2503-1 | 71335250301 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2503-1) | 2024-09-23 | No | No | Historical |
| 71335-2503-2 | 71335250302 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2503-2) | 2024-09-23 | No | No | Historical |
| 71335-2503-3 | 71335250303 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2503-3) | 2024-09-23 | No | No | Historical |
| 71335-2503-4 | 71335250304 | 15 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2503-4) | 2024-09-23 | No | No | Historical |
| 71335-2503-5 | 71335250305 | 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2503-5) | 2024-09-23 | No | No | Historical |
| 71335-2503-6 | 71335250306 | 28 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2503-6) | 2024-09-23 | No | No | Historical |
| 71335-2503-7 | 71335250307 | 10 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2503-7) | 2024-09-23 | No | No | Historical |