Drug application
SUCRALFATE (SUCRALFATE)
Drugs@FDA ANDA 212141 · GLENMARK PHARMS LTD
Key facts
| Drug name | SUCRALFATE |
|---|---|
| Active ingredients | SUCRALFATE |
| Application type | ANDA |
| Application number | 212141 |
| Company | GLENMARK PHARMS LTD |
| Dosage forms | SUSPENSION, ORAL |
| Strength | 1GM/10ML |
| Marketing status | Prescription |
| TE codes | AB |
| Reference listed drug | No |
| Latest submission status date | Jan 5, 2026 |
At a glance
- 1–9 Submissions
- None Label versions
- 1–9 Products
- 10–99 Therapeutic equivalents
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About Drugs@FDA applications
Drugs@FDA covers FDA-approved brand-name and generic drugs and therapeutic biologics, with their applications (NDA, ANDA or BLA), products, submissions and labels.