POTASSIUM CHLORIDE
- Product NDC
- 72162-1076
- 11-digit product format
- 721621076
- Labeler code
- 72162
- Product ID
- 72162-1076_ede9d98b-a627-4a32-80fe-11769d5f945a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- POTASSIUM CHLORIDE
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA208864
- Marketing category
- ANDA
- Marketing start
- 2020-01-02
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 600 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 |
|---|
| 72162-1076-1 | 72162107601 | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72162-1076-1) | 2024-04-05 | No | No | Historical |
| 72162-1076-2 | 72162107602 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72162-1076-2) | 2024-04-05 | No | No | Historical |
| 72162-1076-3 | 72162107603 | 360 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72162-1076-3) | 2024-04-05 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| POTASSIUM CHLORIDE | Bryant Ranch Prepack | 2024-04-09 | HUMAN PRESCRIPTION DRUG LABEL | 8 |