KLOR-CON M
- Product NDC
- 66758-170
- 11-digit product format
- 667580170
- Labeler code
- 66758
- Product ID
- 66758-170_4d6dcaa7-b884-4420-9788-f0e16e520eae
- 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
- 2011-01-18
- Marketing end
- 2021-10-31
- 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
- 0000-00-00
- 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 |
|---|
| 66758-170-01 | 66758017001 | 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (66758-170-01) | | 2014-09-01 | 2021-07-31 | No | No | Current |
| 66758-170-13 | 66758017013 | 10 BLISTER PACK in 1 CARTON (66758-170-13) > 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (66758-170-06) | 10 blister pack | 2014-09-01 | 2021-08-31 | No | No | Current |