Sucralfate
- Product NDC
- 70934-525
- 11-digit product format
- 709340525
- Labeler code
- 70934
- Product ID
- 70934-525_a966546f-9a25-5b79-e053-2995a90a3cc8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sucralfate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- NDA018333
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2020-01-24
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| XX73205DH5 | SUCRALFATE | 54182-58-0 | SUCRALFATE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-525-60 | 70934052560 | 60 TABLET in 1 BOTTLE, PLASTIC (70934-525-60) | 60 tablet | 2020-01-24 | 0000-00-00 | No | No | Current |