Sucralfate
- Product NDC
- 70518-3959
- 11-digit product format
- 705183959
- Labeler code
- 70518
- Product ID
- 70518-3959_3bb32136-21fc-131e-e063-6394a90ab24f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sucralfate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA215705
- Marketing category
- ANDA
- Marketing start
- 2023-12-13
- 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 |
|---|
| 70518-3959-0 | 70518395900 | 30 TABLET in 1 BLISTER PACK (70518-3959-0) | 30 tablet | 2023-12-13 | No | No | Historical |