Potassium Chloride
- Product NDC
- 53002-1035
- 11-digit product format
- 530021035
- Labeler code
- 53002
- Product ID
- 53002-1035_0b6d2ba6-7178-458e-82de-df855cca7fef
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- potassium chloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- RPK Pharmaceuticals, Inc.
- 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
- 2021-12-31
- 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 |
|---|
| 53002-1035-0 | 53002103500 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (53002-1035-0) | 2018-10-01 | 0000-00-00 | No | No | Current |
| 53002-1035-3 | 53002103503 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (53002-1035-3) | 2018-10-01 | 0000-00-00 | No | No | Current |