Potassium Chloride
- Product NDC
- 72322-1032
- 11-digit product format
- 723221032
- Labeler code
- 72322
- Product ID
- 72322-1032_ba9457fc-4b87-4b53-e053-2a95a90a82b1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- potassium chloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- AMTA LABS LIMITED
- Application
- ANDA214395
- Marketing category
- ANDA
- Marketing start
- 2021-12-20
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72322-1032-1 | 72322103201 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (72322-1032-1) | 2021-12-20 | 0000-00-00 | No | No | Current |
| 72322-1032-2 | 72322103202 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (72322-1032-2) | 2021-12-20 | 0000-00-00 | No | No | Current |
| 72322-1032-3 | 72322103203 | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (72322-1032-3) | 2021-12-20 | 0000-00-00 | No | No | Current |