Sucralfate 68788-8779
Product NDC
68788-8779- Manufacturer
- Preferred Pharmaceuticals Inc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- December 10, 2024
- Listing Expires
- December 31, 2027
- Application
- ANDA215705
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Sucralfate | 1 g/1 |
Drug Class
Aluminum Complex [EPC]Aluminum Complex [EPC]Organometallic Compounds [CS]
Packaging Options(2)
30 TABLET in 1 BOTTLE (68788-8779-3)
100 TABLET in 1 BOTTLE (68788-8779-9)