KLOR-CON
- Product NDC
- 65084-464
- 11-digit product format
- 650840464
- Labeler code
- 65084
- Product ID
- 65084-464_8262ef8f-1fd8-4869-add2-3f607c32d8bd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- potassium chloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Mckesson Rxpak Inc
- Application
- NDA019123
- Marketing category
- NDA
- Marketing start
- 2014-09-01
- Marketing end
- 0000-00-00
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 600 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record