Potassium Chloride
- Product NDC
- 0904-7086
- 11-digit product format
- 009047086
- Labeler code
- 0904
- Product ID
- 0904-7086_6ae34cdf-4f32-4719-b52a-e2a7612f5f40
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA206347
- Marketing category
- ANDA
- Marketing start
- 2016-01-21
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0904-7086-45 | 00904708645 | 80 BLISTER PACK in 1 CARTON (0904-7086-45) > 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 80 blister pack | 2016-01-21 | 0000-00-00 | No | No | Current |
| 0904-7086-61 | 00904708661 | 100 BLISTER PACK in 1 CARTON (0904-7086-61) > 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 100 blister pack | 2016-01-21 | 0000-00-00 | No | No | Current |