Active Ingredient: CARBAMAZEPINE
Proprietary Name: TEGRETOL
Dosage Form; Route of Administration: SUSPENSION; ORAL
Strength: 100MG/5ML
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AB
Application Number: N018927
Product Number: 001
Approval Date: Dec 18, 1987
Applicant Holder Full Name: NOVARTIS PHARMACEUTICALS CORP
Marketing Status:
Prescription
Patent and Exclusivity Information
