Potassium Chloride
- Product NDC
- 52584-965
- 11-digit product format
- 525840965
- Labeler code
- 52584
- Product ID
- 52584-965_1c3433b5-5bd6-4cb9-ba1c-c5c2b60831de
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- INJECTION, SOLUTION, CONCENTRATE
- Route
- INTRAVENOUS
- Labeler
- General Injectables & Vaccines, Inc
- Application
- ANDA088901
- Marketing category
- ANDA
- Marketing start
- 2010-08-01
- Marketing end
- 2023-04-30
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 2 meq/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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 52584-965-02 | 52584096502 | 1 VIAL in 1 BAG (52584-965-02) > 20 mL in 1 VIAL | 1 vial | 2019-12-13 | 2023-11-30 | No | No | Current |
| 52584-965-05 | 52584096505 | 1 VIAL, SINGLE-DOSE in 1 BAG (52584-965-05) > 5 mL in 1 VIAL, SINGLE-DOSE | | 2010-08-01 | 2023-04-30 | No | No | Current |