Potassium Chloride
- Product NDC
- 68071-4296
- 11-digit product format
- 680714296
- Labeler code
- 68071
- Product ID
- 68071-4296_bb78db1c-926f-f69a-e053-2995a90a0fb7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- NDA019123
- Marketing category
- NDA
- Marketing start
- 1986-04-17
- Marketing end
- 0000-00-00
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 750 mg/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
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 |
|---|
| 68071-4296-3 | 68071429603 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68071-4296-3) | 2018-02-20 | 0000-00-00 | No | No | Current |