Potassium Chloride
- Product NDC
- 70934-443
- 11-digit product format
- 709340443
- Labeler code
- 70934
- Product ID
- 70934-443_b7aefd05-c4be-1788-e053-2995a90aa72f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Potassium Chloride
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA210733
- Marketing category
- ANDA
- Marketing start
- 2019-09-16
- Marketing end
- 0000-00-00
- 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
- 2021-12-31
- 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 |
|---|
| 70934-443-90 | 70934044390 | 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70934-443-90) | 2019-09-16 | 0000-00-00 | No | No | Current |