Orange Book product
NAPROXEN SODIUM 220MG
Orange Book ANDA 074646 · PLD ACQUISITIONS LLC · Discontinued
Key facts
| Proprietary name | NAPROXEN SODIUM |
|---|---|
| Active ingredients | NAPROXEN SODIUM |
| Strength | 220MG |
| Dosage form | TABLET |
| Route | ORAL |
| Application | ANDA074646 |
| Applicant holder | PLD ACQUISITIONS LLC |
| Marketing status | Discontinued |
| Reference listed drug (RLD) | No |
| Reference standard (RS) | No |
| Approval date | Jan 13, 1997 |
At a glance
- 10–99 Marketed products with the same ingredient, strength and form
- 1–9 Products in this application
- No Reference listed drug
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About Orange Book products
The FDA Orange Book lists approved drug products with their therapeutic equivalence (TE) codes, reference listed drugs and marketing status. Products approved before 1982 show an approval date of Jan 1, 1982.