potassium chloride
- Product NDC
- 60760-068
- 11-digit product format
- 607600068
- Labeler code
- 60760
- Product ID
- 60760-068_8d42b556-a37e-06fc-e053-2995a90aecda
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- potassium chloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- ANDA203562
- Marketing category
- ANDA
- Marketing start
- 2019-07-09
- Marketing end
- 0000-00-00
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 1500 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 |
|---|
| 60760-068-30 | 60760006830 | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (60760-068-30) | 2019-07-09 | 0000-00-00 | No | No | Current |