KLOR-CON
- Product NDC
- 55154-0927
- 11-digit product format
- 551540927
- Labeler code
- 55154
- Product ID
- 55154-0927_d361a56f-ef86-4b78-aeda-a9751c489886
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- potassium chloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- NDA019123
- Marketing category
- NDA
- Marketing start
- 2014-09-01
- Marketing end
- 2021-10-31
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 750 mg/1
- Pharmacologic classes
- Potassium Compounds [CS],Potassium Salt [EPC],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA]
- 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 |
|---|
| 55154-0927-0 | 55154092700 | 10 BLISTER PACK in 1 BAG (55154-0927-0) > 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK | 10 blister pack | 2014-09-01 | 2021-10-31 | No | No | Current |