Active Ingredient: METHADONE HYDROCHLORIDE
Proprietary Name: METHADONE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET, FOR SUSPENSION; ORAL
Strength: 40MG
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AA
Application Number: N017058
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: HIKMA PHARMACEUTICALS USA INC
Marketing Status:
Prescription
Patent and Exclusivity Information
