Potassium Chloride
- Product NDC
- 64330-615
- 11-digit product format
- 643300615
- Labeler code
- 64330
- Product ID
- 64330-615_201ac7f7-7746-475c-953b-cc741afd220c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Centaur Pharmaceuticals Private Limited
- Application
- ANDA213588
- Marketing category
- ANDA
- Marketing start
- 2020-08-21
- 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
- 2022-12-31
- 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 |
|---|
| 64330-615-01 | 64330061501 | 100 TABLET in 1 BOTTLE (64330-615-01) | 100 tablet | 2020-08-21 | 0000-00-00 | No | No | Current |