Potassium Chloride
- Product NDC
- 50090-3449
- 11-digit product format
- 500903449
- Labeler code
- 50090
- Product ID
- 50090-3449_20032e80-13ae-4c7f-b02a-54e20f0417de
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA200185
- Marketing category
- ANDA
- Marketing start
- 2011-06-03
- Marketing end
- 0000-00-00
- 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
- 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 |
|---|
| 50090-3449-9 | 50090344909 | 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (50090-3449-9) | 2018-05-04 | 0000-00-00 | No | No | Current |