POTASSIUM CHLORIDE
- Product NDC
- 55154-6999
- 11-digit product format
- 551546999
- Labeler code
- 55154
- Product ID
- 55154-6999_11796698-4626-4912-b584-185003f40317
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- POTASSIUM CHLORIDE
- Dosage form
- INJECTION, SOLUTION, CONCENTRATE
- Route
- INTRAVENOUS
- Labeler
- Cardinal Health
- Application
- ANDA080205
- Marketing category
- ANDA
- Marketing start
- 1972-03-16
- Marketing end
- 0000-00-00
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 149 mg/mL
- 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