Potassium Chloride
- Product NDC
- 52584-651
- 11-digit product format
- 525840651
- Labeler code
- 52584
- Product ID
- 52584-651_e8b57a1d-2182-4c37-976c-cf8df038a209
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- INJECTION, SOLUTION, CONCENTRATE
- Route
- INTRAVENOUS
- Labeler
- General Injectables and Vaccines, Inc.
- Application
- ANDA080205
- Marketing category
- ANDA
- Marketing start
- 2015-11-16
- Marketing end
- 2023-12-01
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 149 mg/mL
- 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
- 0000-00-00
- 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 |
|---|
| 52584-651-06 | 52584065106 | 1 VIAL, SINGLE-DOSE in 1 BAG (52584-651-06) > 1 mL in 1 VIAL, SINGLE-DOSE | 2015-11-16 | 0000-00-00 | No | No | Current |