Active Ingredient: PHENTERMINE HYDROCHLORIDE
Proprietary Name: PHENTERMINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 8MG
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: A083804
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: USL PHARMA INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
