KLOR-CON M20
- Product NDC
- 50090-5612
- 11-digit product format
- 500905612
- Labeler code
- 50090
- Product ID
- 50090-5612_5515e935-7291-48db-a7c2-6f5e4f4cc972
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- potassium chloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA074726
- Marketing category
- ANDA
- Marketing start
- 2011-01-18
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-5612-0 | 50090561200 | 100 BLISTER PACK in 1 CARTON (50090-5612-0) > 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK | 100 blister pack | 2021-08-12 | 0000-00-00 | No | No | Current |