POTASSIUM CHLORIDE
- Product NDC
- 72789-002
- 11-digit product format
- 727890002
- Labeler code
- 72789
- Product ID
- 72789-002_d22cfada-e643-5af4-e053-2995a90acaca
- 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
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72789-002-30 | 72789000230 | 30 CAPSULE in 1 BOTTLE, PLASTIC (72789-002-30) | 30 capsule | 2019-08-13 | 0000-00-00 | No | No | Current |