NDC 71335-2637 – Sucralfate
Sucralfate 1 g/1 · Tablet · Oral
Product NDC71335-2637
Product details
- Brand name
- Sucralfate
- Generic name
- Sucralfate
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- NDA AUTHORIZED GENERIC · NDA018333
- Marketed since
- September 25, 2017
- Listing expires
- December 31, 2026
- Pharmacologic class
- Aluminum Complex
Active ingredients
- Sucralfate 1 g/1
Package NDC codes (9)
| Package NDC | Description | Since |
|---|---|---|
| 71335-2637-0 | 28 TABLET in 1 BOTTLE (71335-2637-0) | Jun 2, 2025 |
| 71335-2637-1 | 100 TABLET in 1 BOTTLE (71335-2637-1) | Jun 2, 2025 |
| 71335-2637-2 | 60 TABLET in 1 BOTTLE (71335-2637-2) | Jun 2, 2025 |
| 71335-2637-3 | 30 TABLET in 1 BOTTLE (71335-2637-3) | Jun 2, 2025 |
| 71335-2637-4 | 20 TABLET in 1 BOTTLE (71335-2637-4) | Jun 2, 2025 |
| 71335-2637-6 | 150 TABLET in 1 BOTTLE (71335-2637-6) | Jun 2, 2025 |
| 71335-2637-7 | 90 TABLET in 1 BOTTLE (71335-2637-7) | Jun 2, 2025 |
| 71335-2637-8 | 40 TABLET in 1 BOTTLE (71335-2637-8) | Jun 2, 2025 |
| 71335-2637-9 | 120 TABLET in 1 BOTTLE (71335-2637-9) | Jun 2, 2025 |
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