Active Ingredient: CHLORPHENTERMINE HYDROCHLORIDE
Proprietary Name: PRE-SATE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 65MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N014696
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: PARKE DAVIS DIV WARNER LAMBERT CO
Marketing Status:
Discontinued
Patent and Exclusivity Information
