Sucralfate
- Product NDC
- 51407-881
- 11-digit product format
- 514070881
- Labeler code
- 51407
- Product ID
- 51407-881_15ad3251-d853-7efe-e063-6294a90a0d34
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sucralfate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Golden State Medical Supply, Inc.
- Application
- ANDA074415
- Marketing category
- ANDA
- Marketing start
- 1998-06-08
- 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 |
|---|
| 51407-881-90 | 51407088190 | 90 TABLET in 1 BOTTLE, PLASTIC (51407-881-90) | 90 tablet | 2024-03-16 | No | No | Historical |