Sucralfate 51655-0031
Product NDC
51655-0031- Manufacturer
- Northwind Health Company, Llc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- February 9, 2015
- Listing Expires
- December 31, 2027
- Application
- ANDA070848
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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, DISPENSING (51655-031-52)