Potassium Chloride Extended-Release
- Product NDC
- 71335-2866
- 11-digit product format
- 713352866
- Labeler code
- 71335
- Product ID
- 71335-2866_af8e2fea-aa03-4fc5-8e9a-2c10ef9ba59e
- 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
openFDA Listing Details
- Product ID
- 71335-2866_af8e2fea-aa03-4fc5-8e9a-2c10ef9ba59e
- Product type
- HUMAN PRESCRIPTION DRUG
- Finished product
- Yes
- Brand name base
- Potassium Chloride Extended-Release
- Generic name
- Potassium Chloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Marketing start
- 2019-11-20
- Marketing category
- ANDA
- Application number
- ANDA076368
- 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]
- Listing expiration
- 2026-12-31
openFDA Active Ingredients
| Ingredient | Strength |
|---|
| POTASSIUM CHLORIDE | 750 mg/1 |
openFDA Harmonized Identifiers
| Field | Values |
|---|
| Unii | 660YQ98I10 |
| Rxcui | 1801298 |
| Spl Set Id | 6fc9eef0-3dfc-4344-85c7-9f11d9b99b65 |
| Manufacturer Name | Bryant Ranch Prepack |
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 |
|---|
| 71335-2866-1 | 71335286601 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-2866-1) | 2025-11-06 | No | No | Current |