Sucralfate
- Product NDC
- 51655-031
- 11-digit product format
- 516550031
- Labeler code
- 51655
- Product ID
- 51655-031_46ddb2f3-3673-237a-e063-6294a90aa52c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sucralfate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Northwind Health Company, LLC
- Application
- ANDA070848
- Marketing category
- ANDA
- Marketing start
- 2015-02-09
- 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#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51655-031-52 | Sucralfate | 30 in 1 BOTTLE, DISPENSING | TABLET | 30 | | 3 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51655-031 | SUCRALFATE TABLET [NORTHWIND PHARMACEUTICALS, LLC] | 2 | Current NDC, Legacy NDC, 1 package rows | 20230207_464bf611-4dbb-4707-b9dd-39ca178ed4bf.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 |
|---|
| 51655-031-52 | 51655003152 | 30 TABLET in 1 BOTTLE, DISPENSING (51655-031-52) | 30 tablet | 2015-02-09 | No | No | Current |