Active Ingredient: TOLMETIN SODIUM
Proprietary Name: TOLMETIN SODIUM
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 600MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A074399
Product Number: 001
Approval Date: Mar 28, 1996
Applicant Holder Full Name: COSETTE PHARMACEUTICALS INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
