NDC 71335-2114 – Sucralfate
Sucralfate 1 g/1 · Tablet · Oral
Product NDC71335-2114
Product details
- Brand name
- Sucralfate
- Generic name
- Sucralfate
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA074415
- Marketed since
- February 17, 2020
- Listing expires
- December 31, 2026
- Pharmacologic class
- Aluminum Complex
Active ingredients
- Sucralfate 1 g/1
Package NDC codes (9)
| Package NDC | Description | Since |
|---|---|---|
| 71335-2114-0 | 28 TABLET in 1 BOTTLE, PLASTIC (71335-2114-0) | Jun 20, 2022 |
| 71335-2114-1 | 100 TABLET in 1 BOTTLE, PLASTIC (71335-2114-1) | Jun 20, 2022 |
| 71335-2114-2 | 60 TABLET in 1 BOTTLE, PLASTIC (71335-2114-2) | Jun 20, 2022 |
| 71335-2114-3 | 30 TABLET in 1 BOTTLE, PLASTIC (71335-2114-3) | Jun 20, 2022 |
| 71335-2114-4 | 20 TABLET in 1 BOTTLE, PLASTIC (71335-2114-4) | Jun 20, 2022 |
| 71335-2114-6 | 150 TABLET in 1 BOTTLE, PLASTIC (71335-2114-6) | Jun 20, 2022 |
| 71335-2114-7 | 90 TABLET in 1 BOTTLE, PLASTIC (71335-2114-7) | Jun 20, 2022 |
| 71335-2114-8 | 40 TABLET in 1 BOTTLE, PLASTIC (71335-2114-8) | Jun 20, 2022 |
| 71335-2114-9 | 120 TABLET in 1 BOTTLE, PLASTIC (71335-2114-9) | Jun 20, 2022 |
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