Sucralfate
- Product NDC
- 50090-5287
- 11-digit product format
- 500905287
- Labeler code
- 50090
- Product ID
- 50090-5287_270e52df-d16b-4a96-b751-ff580c2f00c4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sucralfate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- NDA018333
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2017-09-25
- 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
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/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | XX73205DH5 |
| Rxcui | 314234 |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-5287-0 | Sucralfate | 60 in 1 BOTTLE | TABLET | 60 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-5287 | SUCRALFATE TABLET [A-S MEDICATION SOLUTIONS] | 5 | Current NDC, Legacy NDC, 1 package rows | 20230630_793d033d-d341-4910-8dda-d43d8fd03a4d.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 |
|---|
| 50090-5287-0 | 50090528700 | 60 TABLET in 1 BOTTLE (50090-5287-0) | 60 tablet | 2020-10-22 | 0000-00-00 | No | No | Current |