Active Ingredient: PHENTERMINE HYDROCHLORIDE
Proprietary Name: PHENTERMINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 37.5MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A088917
Product Number: 001
Approval Date: Jul 17, 1985
Applicant Holder Full Name: USL PHARMA INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
