Potassium Chloride
- Product NDC
- 51407-120
- 11-digit product format
- 514070120
- Labeler code
- 51407
- Product ID
- 51407-120_99dab8b2-1b4c-e2e8-e053-2a95a90ae1eb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- CAPSULE, COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA203002
- Marketing category
- ANDA
- Marketing start
- 2015-12-18
- Marketing end
- 0000-00-00
- 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
- 2020-12-31
- 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 |
|---|
| 51407-120-01 | 51407012001 | 100 CAPSULE, COATED, EXTENDED RELEASE in 1 BOTTLE (51407-120-01) | 2018-06-11 | 0000-00-00 | No | No | Current |
| 51407-120-05 | 51407012005 | 500 CAPSULE, COATED, EXTENDED RELEASE in 1 BOTTLE (51407-120-05) | 2018-06-11 | 0000-00-00 | No | No | Current |