Potassium Chloride Extended-Release 70010-0135
Product NDC
70010-0135- Manufacturer
- Granules Pharmaceuticals Inc.
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 30, 2021
- Listing Expires
- December 31, 2027
- Application
- ANDA214452
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Potassium Chloride | 1500 mg/1 |
Drug Class
Increased Large Intestinal Motility [PE]Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]Osmotic Activity [MoA]
Packaging Options(3)
100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70010-135-01)
500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70010-135-05)
1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (70010-135-10)