Potassium Chloride Extended-Release
- Product NDC
- 72162-1786
- 11-digit product format
- 721621786
- Labeler code
- 72162
- Product ID
- 72162-1786_000215d5-841c-4f90-bfd4-de560e5e042a
- 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 |
|---|
| 72162-1786-0 | 72162178600 | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1786-0) | 2024-04-04 | No | No | Historical |
| 72162-1786-1 | 72162178601 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1786-1) | 2024-04-04 | No | No | Historical |
| 72162-1786-2 | 72162178602 | 180 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1786-2) | 2024-04-04 | No | No | Historical |
| 72162-1786-4 | 72162178604 | 360 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1786-4) | 2024-04-04 | No | No | Historical |
| 72162-1786-5 | 72162178605 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1786-5) | 2024-04-04 | No | No | Historical |
| 72162-1786-7 | 72162178607 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1786-7) | 2024-06-18 | No | No | Historical |
| 72162-1786-9 | 72162178609 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (72162-1786-9) | 2024-04-04 | No | No | Historical |