KLOR-CON
- Product NDC
- 66758-110
- 11-digit product format
- 667580110
- Labeler code
- 66758
- Product ID
- 66758-110_b6795c1c-762b-4589-a49c-cc2d6854ba65
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- potassium chloride
- Dosage form
- TABLET, FILM COATED, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Sandoz Inc.
- Application
- NDA019123
- Marketing category
- NDA
- Marketing start
- 2014-09-01
- Marketing end
- 2021-09-30
- Substance
- POTASSIUM CHLORIDE
- Active strength
- 600 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 |
|---|
| 66758-110-01 | 66758011001 | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (66758-110-01) | | 2014-09-01 | 2021-09-30 | No | No | Current |
| 66758-110-05 | 66758011005 | 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (66758-110-05) | | 2014-09-01 | 2021-05-31 | No | No | Current |
| 66758-110-13 | 66758011013 | 10 BLISTER PACK in 1 CARTON (66758-110-13) > 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (66758-110-06) | 10 blister pack | 2014-09-01 | 2021-09-30 | No | No | Current |