Active Ingredient: TRAMADOL HYDROCHLORIDE
Proprietary Name: TRAMADOL HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 50MG
Reference Listed Drug: No
Reference Standard: Yes
TE Code: AB
Application Number: A075964
Product Number: 001
Approval Date: Jun 19, 2002
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES INC
Marketing Status:
Prescription
Patent and Exclusivity Information