Drug application
NAPROXEN SODIUM (NAPROXEN SODIUM)
Drugs@FDA ANDA 208363 · PURACAP PHARM LLC
Key facts
| Drug name | NAPROXEN SODIUM |
|---|---|
| Active ingredients | NAPROXEN SODIUM |
| Application type | ANDA |
| Application number | 208363 |
| Company | PURACAP PHARM LLC |
| Dosage forms | CAPSULE, ORAL |
| Strength | EQ 200MG BASE |
| Marketing status | Over-the-counter |
| Reference listed drug | No |
| Latest submission status date | Mar 15, 2018 |
At a glance
- 1–9 Submissions
- 1–9 Supplements
- None Label versions
- 1–9 Products
- None 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: