Active Ingredient: TOLMETIN SODIUM
Proprietary Name: TOLECTIN
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 200MG BASE
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N017628
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: ORTHO MCNEIL JANSSEN PHARMACEUTICALS INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
