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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 .