Active Ingredient: TOLMETIN SODIUM
Proprietary Name: TOLECTIN DS
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: EQ 400MG BASE
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N018084
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
