Sucralfate 81033-0149
Product NDC
81033-0149- Manufacturer
- Kesin Pharma Corporation
- Dosage Form
- Suspension
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 1, 2024
- Listing Expires
- December 31, 2026
- Application
- ANDA216474
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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(2)
40 CUP, UNIT-DOSE in 1 CARTON (81033-149-44) / 10 mL in 1 CUP, UNIT-DOSE (81033-149-10)
100 CUP, UNIT-DOSE in 1 CASE (81033-149-52) / 10 mL in 1 CUP, UNIT-DOSE (81033-149-10)