Potassium Chloride
- Product NDC
- 63629-2703
- 11-digit product format
- 636292703
- Labeler code
- 63629
- Product ID
- 63629-2703_6766515e-12f9-4c45-977c-e099c74fe931
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- potassium chloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA076368
- Marketing category
- ANDA
- Marketing start
- 2004-08-18
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-2703-1 | 63629270301 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-2703-1) | 2007-12-24 | 0000-00-00 | No | No | Current |
| 63629-2703-2 | 63629270302 | 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-2703-2) | 2007-12-24 | 0000-00-00 | No | No | Current |
| 63629-2703-3 | 63629270303 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-2703-3) | 2007-12-24 | 0000-00-00 | No | No | Current |
| 63629-2703-4 | 63629270304 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-2703-4) | 2007-12-24 | 0000-00-00 | No | No | Current |
| 63629-2703-5 | 63629270305 | 15 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-2703-5) | 2005-01-12 | 0000-00-00 | No | No | Current |
| 63629-2703-6 | 63629270306 | 7 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-2703-6) | 2005-01-12 | 0000-00-00 | No | No | Current |
| 63629-2703-7 | 63629270307 | 10 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-2703-7) | 2021-12-22 | 0000-00-00 | No | No | Current |