Potassium Chloride
- Product NDC
- 42543-126
- 11-digit product format
- 425430126
- Labeler code
- 42543
- Product ID
- 42543-126_0e87ef4a-0108-4329-8ccb-64b4f1597c17
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Vensun Pharmaceuticals, Inc.
- Application
- ANDA206630
- Marketing category
- ANDA
- Marketing start
- 2019-05-20
- Marketing end
- 0000-00-00
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 1500 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record