Potassium Chloride
- Product NDC
- 55154-3328
- 11-digit product format
- 551543328
- Labeler code
- 55154
- Product ID
- 55154-3328_25080250-5ac5-4b72-8dfd-79dd9742097d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- potassium chloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA077419
- Marketing category
- ANDA
- Marketing start
- 2009-08-25
- Marketing end
- 2020-12-31
- 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