Potassium Chloride
- Product NDC
- 68084-360
- 11-digit product format
- 680840360
- Labeler code
- 68084
- Product ID
- 68084-360_d4ca9a3b-b8cd-4879-e053-2995a90a30ff
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- potassium chloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA076368
- Marketing category
- ANDA
- Marketing start
- 2009-12-01
- Marketing end
- 0000-00-00
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 20 meq/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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68084-360-09 | 68084036009 | 80 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-360-09) > 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (68084-360-11) | 80 blister pack | 2019-02-09 | 0000-00-00 | No | No | Current |