Potassium Chloride
- Product NDC
- 69680-134
- 11-digit product format
- 696800134
- Labeler code
- 69680
- Product ID
- 69680-134_c5f69d55-8a9e-4227-b3d6-728df4cd0eb2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Vitruvias Therapeutics
- Application
- ANDA209688
- Marketing category
- ANDA
- Marketing start
- 2020-07-01
- Marketing end
- 0000-00-00
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 1500 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 |
|---|
| 69680-134-00 | 69680013400 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (69680-134-00) | 2020-07-01 | 0000-00-00 | No | No | Current |
| 69680-134-92 | 69680013492 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (69680-134-92) | 2020-07-01 | 0000-00-00 | No | No | Current |