Potassium Chloride
- Product NDC
- 43063-829
- 11-digit product format
- 430630829
- Labeler code
- 43063
- Product ID
- 43063-829_a071b7e4-0c5f-44cf-e053-2a95a90ac67d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA074726
- Marketing category
- ANDA
- Marketing start
- 1998-11-20
- 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
- 2021-12-31
- 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 |
|---|
| 43063-829-01 | 43063082901 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43063-829-01) | 2018-01-31 | 0000-00-00 | No | No | Current |