Active Ingredient: TRAMADOL HYDROCHLORIDE
Proprietary Name: TRAMADOL HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 50MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A075968
Product Number: 001
Approval Date: Jun 25, 2002
Applicant Holder Full Name: GRAVITI PHARMACEUTICALS PRIVATE LTD
Marketing Status:
Discontinued
Patent and Exclusivity Information