Potassium Chloride
- Product NDC
- 0615-8336
- 11-digit product format
- 006158336
- Labeler code
- 0615
- Product ID
- 0615-8336_8f5d13e7-80e1-4764-917c-5eaf0afa556e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, LLC dba Vangard Labs
- Application
- ANDA206347
- Marketing category
- ANDA
- Marketing start
- 2016-01-21
- Marketing end
- 2022-03-31
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 10 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
- 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 |
|---|
| 0615-8336-05 | 00615833605 | 15 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0615-8336-05) | 2020-03-18 | 0000-00-00 | No | No | Current |
| 0615-8336-39 | 00615833639 | 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0615-8336-39) | 2020-03-18 | 0000-00-00 | No | No | Current |