Potassium Chloride
- Product NDC
- 66267-681
- 11-digit product format
- 662670681
- Labeler code
- 66267
- Product ID
- 66267-681_b9bd9cdd-3573-65d3-e053-2995a90a1e3a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- potassium chloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA076368
- Marketing category
- ANDA
- Marketing start
- 2004-08-18
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 66267-681-30 | 66267068130 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (66267-681-30) | 2016-12-28 | 0000-00-00 | No | No | Current |
| 66267-681-60 | 66267068160 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (66267-681-60) | 2016-12-28 | 0000-00-00 | No | No | Current |