Active Ingredient: TILUDRONATE DISODIUM
Proprietary Name: SKELID
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 200MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N020707
Product Number: 001
Approval Date: Mar 7, 1997
Applicant Holder Full Name: SANOFI AVENTIS US LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information
