Drug application
PLERIXAFOR (PLERIXAFOR)
Drugs@FDA ANDA 205182 · DR REDDYS
Key facts
| Drug name | PLERIXAFOR |
|---|---|
| Active ingredients | PLERIXAFOR |
| Application type | ANDA |
| Application number | 205182 |
| Company | DR REDDYS |
| Dosage forms | SOLUTION, SUBCUTANEOUS |
| Strength | 24MG/1.2ML (20MG/ML) |
| Marketing status | Prescription |
| TE codes | AP |
| Reference listed drug | No |
| Latest submission status date | Jul 24, 2023 |
At a glance
- 1–9 Submissions
- 1–9 Supplements
- None Label versions
- 1–9 Products
- 10–99 Therapeutic equivalents
- Yes FDA letters on file
- No 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: