Active Ingredient: NAPROXEN
Proprietary Name: NAPROXEN
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 250MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A074110
Product Number: 001
Approval Date: Oct 30, 1992
Applicant Holder Full Name: HAMILTON PHARMACEUTICALS LTD
Marketing Status:
Discontinued
Patent and Exclusivity Information