Sucralfate
- Product NDC
- 68071-3812
- 11-digit product format
- 680713812
- Labeler code
- 68071
- Product ID
- 68071-3812_31a7e09b-5fe1-f1fc-e063-6394a90a63d9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sucralfate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA215705
- Marketing category
- ANDA
- Marketing start
- 2023-05-20
- 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 |
|---|
| 68071-3812-3 | 68071381203 | 30 TABLET in 1 BOTTLE (68071-3812-3) | 30 tablet | 2025-03-19 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Sucralfate Tablets USP, 1g | NuCare Pharmaceuticals, Inc. | 2025-03-19 | HUMAN PRESCRIPTION DRUG LABEL | 1 |