Active Ingredient: PHENTERMINE HYDROCHLORIDE
Proprietary Name: PHENTERMINE HYDROCHLORIDE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 15MG
Reference Listed Drug: No
Reference Standard: No
TE Code: AA
Application Number: A204318
Product Number: 001
Approval Date: Nov 9, 2016
Applicant Holder Full Name: AUROLIFE PHARMA LLC
Marketing Status:
Prescription
Patent and Exclusivity Information
