Sucralfate
- Product NDC
- 68788-8779
- 11-digit product format
- 687888779
- Labeler code
- 68788
- Product ID
- 68788-8779_657d271c-f93e-4356-a043-e8c383b4a023
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sucralfate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc
- Application
- ANDA215705
- Marketing category
- ANDA
- Marketing start
- 2024-12-10
- Substance
- SUCRALFATE
- Active strength
- 1 g/1
- Pharmacologic classes
- Aluminum Complex [EPC], Organometallic Compounds [CS]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Sucralfate
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SUCRALFATE | 1 g/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | XX73205DH5 |
| Rxcui | 314234 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68788-8779-3 | Sucralfate | 30 in 1 BOTTLE | TABLET | 30 | | 2 |
| 68788-8779-9 | Sucralfate | 100 in 1 BOTTLE | TABLET | 100 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68788-8779 | SUCRALFATE TABLET [PREFERRED PHARMACEUTICALS INC] | 1 | Current NDC, 2 package rows | 20241212_a434bf8f-cc60-4d84-a9a4-61c3ff6b700e.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 68788-8779-3 | 68788877903 | 30 TABLET in 1 BOTTLE (68788-8779-3) | 30 tablet | 2024-12-10 | No | No | Historical |
| 68788-8779-9 | 68788877909 | 100 TABLET in 1 BOTTLE (68788-8779-9) | 100 tablet | 2024-12-10 | No | No | Historical |