Potassium Chloride
- Product NDC
- 68071-4708
- 11-digit product format
- 680714708
- Labeler code
- 68071
- Product ID
- 68071-4708_bb8bf871-ebe5-60d7-e053-2a95a90a2032
- 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 |
|---|
| 68071-4708-9 | 68071470809 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68071-4708-9) | 2019-01-11 | 0000-00-00 | No | No | Current |