Active Ingredient: PHENTERMINE HYDROCHLORIDE
Proprietary Name: PHENTERMINE HYDROCHLORIDE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 30MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A088797
Product Number: 001
Approval Date: Dec 10, 1984
Applicant Holder Full Name: USL PHARMA INC
Marketing Status:
Discontinued
Patent and Exclusivity Information