Sucralfate
- Product NDC
- 50268-745
- 11-digit product format
- 502680745
- Labeler code
- 50268
- Product ID
- 50268-745_4510a8c1-2007-1ac1-e063-6294a90a1375
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sucralfate Oral
- Dosage form
- SUSPENSION
- Route
- ORAL
- Labeler
- AvPAK
- Application
- ANDA209356
- Marketing category
- ANDA
- Marketing start
- 2022-08-31
- 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Sucralfate
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SUCRALFATE | 1 g/10mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | XX73205DH5 |
| Rxcui | 313123 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50268-745-11 | Sucralfate | 10 mL in 1 CUP | SUSPENSION | 10 | | 4 |
| 50268-745-14 | Sucralfate | 40 in 1 BOX | SUSPENSION | 40 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50268-745 | SUCRALFATE (SUCRALFATE ORAL) SUSPENSION [AVPAK] | 3 | Current NDC, Legacy NDC, 2 package rows | 20240110_e78ef7d4-faa7-aebf-e053-2995a90a6f84.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50268-745-11 | 50268074511 | 10 mL in 1 CUP | 10 ml | | | | | Historical |
| 50268-745-14 | 50268074514 | 40 CUP in 1 BOX (50268-745-14) / 10 mL in 1 CUP (50268-745-11) | 40 cup | 2022-08-31 | 0000-00-00 | No | No | Current |