Sucralfate
- Product NDC
- 53808-0797
- 11-digit product format
- 538080797
- Labeler code
- 53808
- Product ID
- 53808-0797_bc8c902a-bbb9-46fb-ba2f-0da5862699ac
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- SUCRALFATE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- State of Florida DOH Central Pharmacy
- Application
- ANDA070848
- Marketing category
- ANDA
- Marketing start
- 2009-07-01
- Marketing end
- 0000-00-00
- Substance
- SUCRALFATE
- Active strength
- 1 g/1
- Pharmacologic classes
- Aluminum Complex [EPC],Organometallic Compounds [CS]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- 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 |
|---|
| 53808-0797-1 | Sucralfate | 30 in 1 BLISTER PACK | TABLET | 30 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53808-0797 | SUCRALFATE TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 1 | Legacy NDC, 1 package rows | 20100614_04e60cc5-bdce-4b76-9ec4-3c531fec081d.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 53808-0797-1 | 53808079701 | 30 in 1 BLISTER PACK | Historical |