Potassium Chloride
- Product NDC
- 0615-8314
- 11-digit product format
- 006158314
- Labeler code
- 0615
- Product ID
- 0615-8314_4107124e-1af8-4764-870a-bd8c6ba13bbf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- potassium chloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- NCS HealthCare of KY, Inc dba Vangard Labs
- Application
- ANDA076368
- Marketing category
- ANDA
- Marketing start
- 2004-08-18
- Marketing end
- 2022-01-31
- 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
- 0000-00-00
- 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 |
|---|
| 0615-8314-05 | 00615831405 | 15 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0615-8314-05) | | 2019-08-07 | 2022-01-31 | No | No | Current |
| 0615-8314-30 | 00615831430 | 6 BLISTER PACK in 1 BOX, UNIT-DOSE (0615-8314-30) > 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 6 blister pack | 2019-07-29 | 2022-01-31 | No | No | Current |
| 0615-8314-39 | 00615831439 | 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0615-8314-39) | | 2019-08-07 | 2022-01-31 | No | No | Current |