Potassium Chloride
- Product NDC
- 55154-4158
- 11-digit product format
- 551544158
- Labeler code
- 55154
- Product ID
- 55154-4158_83ef4d53-9ab8-47f6-af45-155ea3fed95b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Cardinal Health 107, LLC
- 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
- Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 55154-4158-0 | 55154415800 | 10 BLISTER PACK in 1 BAG (55154-4158-0) > 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 10 blister pack | 2022-05-12 | 0000-00-00 | No | No | Current |