Potassium Chloride
- Product NDC
- 0615-7940
- 11-digit product format
- 006157940
- Labeler code
- 0615
- Product ID
- 0615-7940_e25b307e-4f21-4d11-9994-bed5f66888c6
- 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
- 2021-07-31
- 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 |
|---|
| 0615-7940-05 | 00615794005 | 15 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0615-7940-05) | | 2016-04-28 | 2021-07-31 | No | No | Current |
| 0615-7940-30 | 00615794030 | 6 BLISTER PACK in 1 BOX, UNIT-DOSE (0615-7940-30) > 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 6 blister pack | 2016-04-26 | 2021-07-31 | No | No | Current |
| 0615-7940-39 | 00615794039 | 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (0615-7940-39) | | 2016-04-28 | 2021-07-31 | No | No | Current |