Drug application
SOLU-MEDROL (METHYLPREDNISOLONE SODIUM SUCCINATE)
Drugs@FDA NDA 011856 · PHARMACIA AND UPJOHN
Key facts
| Drug name | SOLU-MEDROL |
|---|---|
| Active ingredients | METHYLPREDNISOLONE SODIUM SUCCINATE |
| Application type | NDA |
| Application number | 011856 |
| Company | PHARMACIA AND UPJOHN |
| Dosage forms | INJECTABLE, INJECTION |
| Strength | EQ 40MG BASE/VIAL |
| Marketing status | Prescription |
| TE codes | AP |
| Reference listed drug | Yes |
| Latest submission class | Type 2 - New Active Ingredient |
| Latest submission status date | May 18, 1959 |
At a glance
- 1–9 Submissions
- 10–99 Supplements
- 10–99 Label versions
- 1–9 Products
- 1–9 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.
Source: U.S. Food and Drug Administration (FDA), Drugs@FDA · Source date: