Sucralfate 68071-3812
Product NDC
68071-3812- Manufacturer
- Nucare Pharmaceuticals, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 20, 2023
- Listing Expires
- December 31, 2026
- 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(1)
30 TABLET in 1 BOTTLE (68071-3812-3)