Potassium Chloride
- Product NDC
- 60760-600
- 11-digit product format
- 607600600
- Labeler code
- 60760
- Product ID
- 60760-600_7c267075-42e2-eb7c-e053-2991aa0a8658
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- St Marys Medical Park Pharmacy
- Application
- NDA018279
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2013-05-15
- 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
- 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 |
|---|
| 60760-600-30 | 60760060030 | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (60760-600-30) | 2013-05-15 | 0000-00-00 | No | No | Current |
| 60760-600-90 | 60760060090 | 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (60760-600-90) | 2015-11-16 | 0000-00-00 | No | No | Current |