Drug application
CEFTIN (CEFUROXIME AXETIL)
Drugs@FDA NDA 050605 · GLAXOSMITHKLINE
Key facts
| Drug name | CEFTIN |
|---|---|
| Active ingredients | CEFUROXIME AXETIL |
| Application type | NDA |
| Application number | 050605 |
| Company | GLAXOSMITHKLINE |
| Dosage forms | TABLET, ORAL |
| Strength | EQ 125MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** |
| Marketing status | Discontinued |
| Reference listed drug | Yes |
| Latest submission class | Type 2 - New Active Ingredient |
| Latest submission status date | Dec 28, 1987 |
At a glance
- 1–9 Submissions
- 10–99 Supplements
- 10–99 Label versions
- 1–9 Products
- None 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: