Potassium Chloride
- Product NDC
- 0615-8212
- 11-digit product format
- 006158212
- Labeler code
- 0615
- Product ID
- 0615-8212_345064b7-35e4-435b-8c30-fb30033437a6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- CAPSULE, COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, LLC dba Vangard Labs
- Application
- ANDA203002
- Marketing category
- ANDA
- Marketing start
- 2016-01-18
- Marketing end
- 2024-07-31
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 10 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
- 0000-00-00
- 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 |
|---|
| 0615-8212-05 | 00615821205 | 15 CAPSULE, COATED, EXTENDED RELEASE in 1 BLISTER PACK (0615-8212-05) | 2018-05-03 | 2024-07-31 | No | No | Current |
| 0615-8212-39 | 00615821239 | 30 CAPSULE, COATED, EXTENDED RELEASE in 1 BLISTER PACK (0615-8212-39) | 2018-05-03 | 2024-07-31 | No | No | Current |