Sucralfate
- Product NDC
- 66267-596
- 11-digit product format
- 662670596
- Labeler code
- 66267
- Product ID
- 66267-596_b8a7bb10-159c-39f0-e053-2a95a90a512a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sucralfate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA070848
- Marketing category
- ANDA
- Marketing start
- 1996-11-11
- Marketing end
- 0000-00-00
- Substance
- SUCRALFATE
- Active strength
- 1 g/1
- Pharmacologic classes
- Aluminum Complex [EPC],Organometallic Compounds [CS]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
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 |
|---|
| 66267-596-30 | Sucralfate | 30 in 1 BOTTLE | TABLET | 30 | | 3 |
| 66267-596-60 | Sucralfate | 60 in 1 BOTTLE | TABLET | 60 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 66267-596 | SUCRALFATE TABLET [NUCARE PHARMACEUTICALS, INC.] | 3 | Legacy NDC, 2 package rows | 20210112_44ab9815-39f4-1463-e054-00144ff8d46c.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 |
|---|
| 66267-596-30 | 66267059630 | 30 TABLET in 1 BOTTLE (66267-596-30) | 30 tablet | 2016-12-27 | 0000-00-00 | No | No | Current |
| 66267-596-60 | 66267059660 | 60 TABLET in 1 BOTTLE (66267-596-60) | 60 tablet | 2016-12-27 | 0000-00-00 | No | No | Current |