POTASSIUM CHLORIDE
- Product NDC
- 48433-217
- 11-digit product format
- 484330217
- Labeler code
- 48433
- Product ID
- 48433-217_2b722f76-6e6e-4815-bf70-a17fad30a680
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- POTASSIUM CHLORIDE
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Safecor Health, LLC
- Application
- ANDA211067
- Marketing category
- ANDA
- Marketing start
- 2019-05-24
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 48433-217-40 | 48433021740 | 40 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (48433-217-40) > 15 mL in 1 CUP, UNIT-DOSE (48433-217-15) | 2019-05-24 | 0000-00-00 | No | No | Current |