Active Ingredient: PHENMETRAZINE HYDROCHLORIDE
Proprietary Name: PRELUDIN
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 25MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N010460
Product Number: 005
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: BOEHRINGER INGELHEIM PHARMACEUTICALS INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
