potassium chloride
- Product NDC
- 68084-419
- 11-digit product format
- 680840419
- Labeler code
- 68084
- Product ID
- 68084-419_66d7a970-d12f-7c88-e053-2a91aa0a9c66
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- potassium chloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- NDA018238
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2012-06-26
- Marketing end
- 2019-08-31
- 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