Active Ingredient: NAPROXEN SODIUM
Proprietary Name: NAPROXEN SODIUM
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 250MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A074106
Product Number: 001
Approval Date: Aug 31, 1993
Applicant Holder Full Name: HAMILTON PHARMACEUTICALS LTD
Marketing Status:
Discontinued
Patent and Exclusivity Information