Potassium Chloride 68462-0472
Product NDC
68462-0472- Manufacturer
- Glenmark Pharmaceuticals Inc., Usa
- Dosage Form
- Tablet, Extended Release
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 26, 2016
- Listing Expires
- December 31, 2026
- Application
- ANDA203562
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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(2)
100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68462-472-01)
500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68462-472-05)