Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 011752

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PRELUDIN (PHENMETRAZINE HYDROCHLORIDE)
50MG
Marketing Status: Discontinued

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

PRELUDIN (PHENMETRAZINE HYDROCHLORIDE)
75MG
Marketing Status: Discontinued

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