Potassium Chloride
- Product NDC
- 49999-740
- 11-digit product format
- 499990740
- Labeler code
- 49999
- Product ID
- 49999-740_04940176-9b6c-4fdb-bd48-11618609f537
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- potassium chloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- 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
- 2020-12-31
- 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 |
|---|
| 49999-740-30 | 49999074030 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (49999-740-30) | 2008-01-31 | 0000-00-00 | No | No | Current |
| 49999-740-90 | 49999074090 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (49999-740-90) | 2008-01-31 | 0000-00-00 | No | No | Current |