Potassium Chloride
- Product NDC
- 72162-2310
- 11-digit product format
- 721622310
- Labeler code
- 72162
- Product ID
- 72162-2310_d914b262-7244-4d71-980d-e5508f994eba
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- POWDER, FOR SOLUTION
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA210200
- Marketing category
- ANDA
- Marketing start
- 2021-01-01
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 1.5 g/1.77g
- 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 | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-2310-1 | 72162231001 | 100 PACKET in 1 CARTON (72162-2310-1) / 1.77 g in 1 PACKET (72162-2310-2) | 100 packet | 2024-05-07 | No | No | Historical |
| 72162-2310-3 | 72162231003 | 30 PACKET in 1 CARTON (72162-2310-3) / 1.77 g in 1 PACKET (72162-2310-4) | 30 packet | 2024-05-07 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Potassium Chloride | Bryant Ranch Prepack | 2024-05-21 | HUMAN PRESCRIPTION DRUG LABEL | 102 |