Potassium Chloride
- Product NDC
- 52584-653
- 11-digit product format
- 525840653
- Labeler code
- 52584
- Product ID
- 52584-653_0fab0a76-aa59-4c1a-adb3-3200cf70f434
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- INJECTION, SOLUTION, CONCENTRATE
- Route
- INTRAVENOUS
- Labeler
- General Injectables & Vaccines, Inc
- Application
- ANDA080205
- Marketing category
- ANDA
- Marketing start
- 2010-08-01
- Marketing end
- 2020-10-01
- 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
- 0000-00-00
- Current FDA listing
- Historical FDA.report record