Sucralfate
- Product NDC
- 82804-063
- 11-digit product format
- 828040063
- Labeler code
- 82804
- Product ID
- 82804-063_a42c5f3d-85f1-485b-91e6-58c25b3ddc71
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sucralfate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA070848
- Marketing category
- ANDA
- Marketing start
- 1996-11-11
- 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 |
|---|
| 82804-063-30 | 82804006330 | 30 TABLET in 1 BOTTLE (82804-063-30) | 30 tablet | 2024-01-30 | No | No | Historical |
| 82804-063-60 | 82804006360 | 60 TABLET in 1 BOTTLE (82804-063-60) | 60 tablet | 2024-01-30 | No | No | Historical |
| 82804-063-90 | 82804006390 | 90 TABLET in 1 BOTTLE (82804-063-90) | 90 tablet | 2024-01-30 | No | No | Historical |