Active Ingredient: BACLOFEN
Proprietary Name: BACLOFEN
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 20MG
Reference Listed Drug: No
Reference Standard: Yes
TE Code: AB
Application Number: A072235
Product Number: 001
Approval Date: Jul 21, 1988
Applicant Holder Full Name: IVAX PHARMACEUTICALS INC SUB TEVA PHARMACEUTICALS USA
Marketing Status:
Prescription
Patent and Exclusivity Information
