Active Ingredient: GABAPENTIN
Proprietary Name: GABAPENTIN
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 600MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AB1
Application Number: A077661
Product Number: 004
Approval Date: Sep 13, 2006
Applicant Holder Full Name: RUBICON RESEARCH PRIVATE LTD
Marketing Status:
Prescription
Patent and Exclusivity Information