Sucralfate 82182-0106
Product NDC
82182-0106- Manufacturer
- Pacific Pharma, Inc.
- Dosage Form
- Suspension
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- February 1, 2024
- Listing Expires
- December 31, 2026
- Application
- NDA019183
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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 (82182-106-14)