Potassium Chloride
- Product NDC
- 60687-533
- 11-digit product format
- 606870533
- Labeler code
- 60687
- Product ID
- 60687-533_9f90d7e2-decb-0dee-e053-2995a90a1a0c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA202868
- Marketing category
- ANDA
- Marketing start
- 2020-02-27
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60687-533-09 | 60687053309 | 80 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-533-09) > 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (60687-533-11) | 80 blister pack | 2020-02-27 | 0000-00-00 | No | No | Current |