Drug application
PREDNISOLONE ACETATE (PREDNISOLONE ACETATE)
Drugs@FDA ANDA 216935 · LUPIN
Key facts
| Drug name | PREDNISOLONE ACETATE |
|---|---|
| Active ingredients | PREDNISOLONE ACETATE |
| Application type | ANDA |
| Application number | 216935 |
| Company | LUPIN |
| Dosage forms | SUSPENSION/DROPS, OPHTHALMIC |
| Strength | 1% |
| Marketing status | Prescription |
| TE codes | AB |
| Reference listed drug | No |
| Latest submission status date | Aug 2, 2024 |
At a glance
- 1–9 Submissions
- None Label versions
- 1–9 Products
- 1–9 Therapeutic equivalents
- No FDA letters on file
- Yes FDA reviews on file
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.
Source: U.S. Food and Drug Administration (FDA), Drugs@FDA · Source date: