Potassium Chloride
- Product NDC
- 0781-5720
- 11-digit product format
- 007815720
- Labeler code
- 0781
- Product ID
- 0781-5720_348185ea-4868-4e07-8e2a-a457bb38bb40
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Sandoz Inc
- Application
- ANDA074726
- Marketing category
- ANDA
- Marketing start
- 1998-11-20
- Marketing end
- 2021-11-30
- 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
- 0000-00-00
- 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 |
|---|
| 0781-5720-01 | 00781572001 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0781-5720-01) | 1998-11-20 | 2021-09-30 | No | No | Current |
| 0781-5720-05 | 00781572005 | 500 TABLET, EXTENDED RELEASE in 1 BOTTLE (0781-5720-05) | 1998-11-20 | 2021-09-30 | No | No | Current |
| 0781-5720-10 | 00781572010 | 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (0781-5720-10) | 1998-11-20 | 2021-08-31 | No | No | Current |