Potassium Chloride
- Product NDC
- 55154-8135
- 11-digit product format
- 551548135
- Labeler code
- 55154
- Product ID
- 55154-8135_bf1ab092-89c3-47e7-920a-1dbd6426bc8b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Cardinal Health
- Application
- ANDA074726
- Marketing category
- ANDA
- Marketing start
- 2009-08-03
- 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
- 2020-12-31
- 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 |
|---|
| 55154-8135-0 | 55154813500 | 10 BLISTER PACK in 1 BAG (55154-8135-0) > 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 10 blister pack | 2009-08-03 | 0000-00-00 | No | No | Current |