Sucralfate
- Product NDC
- 71335-2114
- 11-digit product format
- 713352114
- Labeler code
- 71335
- Product ID
- 71335-2114_fc506a9a-8d99-f22b-e053-6394a90ad6d9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sucralfate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA074415
- Marketing category
- ANDA
- Marketing start
- 2020-02-17
- Substance
- SUCRALFATE
- Active strength
- 1 g/1
- Pharmacologic classes
- Aluminum Complex [EPC], Organometallic Compounds [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| XX73205DH5 | SUCRALFATE | 54182-58-0 | SUCRALFATE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2114-0 | 71335211400 | 28 TABLET in 1 BOTTLE, PLASTIC (71335-2114-0) | 28 tablet | 2022-06-20 | No | No | Historical |
| 71335-2114-1 | 71335211401 | 100 TABLET in 1 BOTTLE, PLASTIC (71335-2114-1) | 100 tablet | 2022-06-20 | No | No | Historical |
| 71335-2114-2 | 71335211402 | 60 TABLET in 1 BOTTLE, PLASTIC (71335-2114-2) | 60 tablet | 2022-06-20 | No | No | Historical |
| 71335-2114-3 | 71335211403 | 30 TABLET in 1 BOTTLE, PLASTIC (71335-2114-3) | 30 tablet | 2022-06-20 | No | No | Historical |
| 71335-2114-4 | 71335211404 | 20 TABLET in 1 BOTTLE, PLASTIC (71335-2114-4) | 20 tablet | 2022-06-20 | No | No | Historical |
| 71335-2114-6 | 71335211406 | 150 TABLET in 1 BOTTLE, PLASTIC (71335-2114-6) | 150 tablet | 2022-06-20 | No | No | Historical |
| 71335-2114-7 | 71335211407 | 90 TABLET in 1 BOTTLE, PLASTIC (71335-2114-7) | 90 tablet | 2022-06-20 | No | No | Historical |
| 71335-2114-8 | 71335211408 | 40 TABLET in 1 BOTTLE, PLASTIC (71335-2114-8) | 40 tablet | 2022-06-20 | No | No | Historical |
| 71335-2114-9 | 71335211409 | 120 TABLET in 1 BOTTLE, PLASTIC (71335-2114-9) | 120 tablet | 2022-06-20 | No | No | Historical |