Active Ingredient: PHENMETRAZINE HYDROCHLORIDE
Proprietary Name: PRELUDIN
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 50MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N011752
Product Number: 004
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: BOEHRINGER INGELHEIM PHARMACEUTICALS INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
Active Ingredient: PHENMETRAZINE HYDROCHLORIDE
Proprietary Name: PRELUDIN
Dosage Form; Route of Administration: TABLET, EXTENDED RELEASE; ORAL
Strength: 75MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N011752
Product Number: 003
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: BOEHRINGER INGELHEIM PHARMACEUTICALS INC
Marketing Status:
Discontinued
Patent and Exclusivity Information