NDC 81033-149 – Sucralfate
Sucralfate 1 g/10mL · Suspension · Oral
Product NDC81033-149
Product details
- Brand name
- Sucralfate
- Generic name
- Sucralfate
- Labeler
- Kesin Pharma Corporation
- Dosage form
- Suspension
- Route
- Oral
- Marketing category
- ANDA · ANDA216474
- Marketed since
- July 1, 2024
- Listing expires
- December 31, 2026
- Pharmacologic class
- Aluminum Complex
Active ingredients
- Sucralfate 1 g/10mL
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 81033-149-44 | 40 CUP, UNIT-DOSE in 1 CARTON (81033-149-44) / 10 mL in 1 CUP, UNIT-DOSE (81033-149-10) | Jul 1, 2024 |
| 81033-149-52 | 100 CUP, UNIT-DOSE in 1 CASE (81033-149-52) / 10 mL in 1 CUP, UNIT-DOSE (81033-149-10) | Jul 1, 2024 |
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