Sucralfate
- Product NDC
- 82804-102
- 11-digit product format
- 828040102
- Labeler code
- 82804
- Product ID
- 82804-102_51459cdb-a04a-49c2-8ee4-8f234f522476
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sucralfate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- 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 |
|---|
| 82804-102-30 | 82804010230 | 30 TABLET in 1 BOTTLE, PLASTIC (82804-102-30) | 30 tablet | 2024-05-06 | No | No | Historical |