Sucralfate
- Product NDC
- 42291-757
- 11-digit product format
- 422910757
- Labeler code
- 42291
- Product ID
- 42291-757_d5c99427-ea8d-47d7-e053-2a95a90a9384
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sucralfate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- AvKARE
- Application
- ANDA070848
- Marketing category
- ANDA
- Marketing start
- 2014-01-17
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 42291-757-50 | 42291075750 | 500 TABLET in 1 BOTTLE (42291-757-50) | 500 tablet | 2014-01-17 | 0000-00-00 | No | No | Current |