Sucralfate
- Product NDC
- 71610-541
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Sucralfate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Application
- ANDA074415
- Marketing category
- ANDA
- Substance
- SUCRALFATE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 71610-541-60 | 90 TABLET in 1 BOTTLE, PLASTIC (71610-541-60) | 2021-04-13 | | No | Historical |
| 71610-541-70 | 120 TABLET in 1 BOTTLE, PLASTIC (71610-541-70) | 2021-04-13 | | No | Historical |
| 71610-541-94 | 360 TABLET in 1 BOTTLE, PLASTIC (71610-541-94) | 2021-04-13 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Sucralfate Tablets, USP 1 gram | Aphena Pharma Solutions - Tennessee, LLC | 2021-05-19 | HUMAN PRESCRIPTION DRUG LABEL | 1 |