Potassium Chloride
- Product NDC
- 17856-1680
- 11-digit product format
- 178561680
- Labeler code
- 17856
- Product ID
- 17856-1680_1eb3d1b6-fab4-495d-b9e5-a6103a1422bc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- POTASSIUM CHLORIDE
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- ATLANTIC BIOLOGICALS CORP.
- Application
- ANDA210766
- Marketing category
- ANDA
- Marketing start
- 2019-04-02
- Marketing end
- 0000-00-00
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 20 meq/15mL
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
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 | Marketing end | Sample | Exclude flag | Status |
|---|
| 17856-1680-1 | 17856168001 | 72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-1680-1) > 15 mL in 1 CUP, UNIT-DOSE (17856-1680-3) | 2022-12-01 | 0000-00-00 | No | No | Current |
| 17856-1680-2 | 17856168002 | 50 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-1680-2) > 30 mL in 1 CUP, UNIT-DOSE (17856-1680-4) | 2022-12-01 | 0000-00-00 | No | No | Current |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Potassium Chloride | ATLANTIC BIOLOGICALS CORP. | 2022-12-01 | HUMAN PRESCRIPTION DRUG LABEL | 2 |