Sucralfate 50742-0386
Product NDC
50742-0386- Manufacturer
- Ingenus Pharmaceuticals, Llc
- Dosage Form
- Suspension
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- November 21, 2024
- Application
- ANDA216726
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Sucralfate | 1 g/10mL |
Drug Class
Aluminum Complex [EPC]Aluminum Complex [EPC]Organometallic Compounds [CS]
Packaging Options(1)
420 mL in 1 BOTTLE (50742-386-42)