Drug application
OXALIPLATIN (OXALIPLATIN)
Drugs@FDA ANDA 091358 · MYLAN LABS LTD
Key facts
| Drug name | OXALIPLATIN |
|---|---|
| Active ingredients | OXALIPLATIN |
| Application type | ANDA |
| Application number | 091358 |
| Company | MYLAN LABS LTD |
| Dosage forms | INJECTABLE, INTRAVENOUS |
| Strength | 50MG/10ML (5MG/ML) |
| Marketing status | Prescription |
| TE codes | AP |
| Reference listed drug | No |
| Latest submission status date | Nov 14, 2017 |
At a glance
- 1–9 Submissions
- 1–9 Supplements
- 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.
Source: U.S. Food and Drug Administration (FDA), Drugs@FDA · Source date: