Aurobindo Receives FDA Approval for Naproxen Oral Suspension USP, 125 mg/5 mL
Published: October 03, 2025
East Windsor, N.J. – Aurobindo Pharma Limited has received final approval from U.S. Food and Drug Administration for its Abbreviated New Drug Application Naproxen Oral Suspension USP, 125 mg/5 mL. Aurobindo Pharma’s Naproxen Oral Suspension, are an AB-rated generic equivalent to the reference listed drug (RLD), Naprosyn Oral Suspension manufactured by Atnahs Pharma US Limited.
Naproxen Oral Suspension are indicated for:
- the relief of the signs and symptoms of:
- rheumatoid arthritis
- osteoarthritis
- ankylosing spondylitis
- polyarticular juvenile idiopathic
- arthritis
- tendonitis
- bursitis
- acute gout
- the management of:
- pain
- primary dysmenorrhea .
