sucralfate
- Product NDC
- 72162-2479
- 11-digit product format
- 721622479
- Labeler code
- 72162
- Product ID
- 72162-2479_4e5200dd-dd65-48be-8dfd-e8411029de9b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sucralfate
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA216474
- Marketing category
- ANDA
- Marketing start
- 2024-07-10
- Substance
- SUCRALFATE
- Active strength
- 1 g/10mL
- 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 |
|---|
| 72162-2479-2 | 72162247902 | 420 mL in 1 BOTTLE (72162-2479-2) | 420 ml | 2025-05-01 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| SUCRALFATE oral suspension | Bryant Ranch Prepack | 2025-05-09 | HUMAN PRESCRIPTION DRUG LABEL | 103 |