POTASSIUM CHLORIDE
- Product NDC
- 43063-978
- 11-digit product format
- 430630978
- Labeler code
- 43063
- Product ID
- 43063-978_d2cdd0d1-03b9-2651-e053-2a95a90a9cff
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- POTASSIUM CHLORIDE
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA208864
- Marketing category
- ANDA
- Marketing start
- 2018-04-01
- Marketing end
- 0000-00-00
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 600 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43063-978-01 | 43063097801 | 100 CAPSULE in 1 BOTTLE, PLASTIC (43063-978-01) | 100 capsule | 2019-04-30 | 0000-00-00 | No | No | Current |