Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

Home | Back to Search Results

Product Details for NDA 019385

Expand all

PERMAX (PERGOLIDE MESYLATE)
EQ 0.05MG BASE
Marketing Status: Discontinued

Active Ingredient: PERGOLIDE MESYLATE
Proprietary Name: PERMAX
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 0.05MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N019385
Product Number: 001
Approval Date: Dec 30, 1988
Applicant Holder Full Name: VALEANT PHARMACEUTICALS INTERNATIONAL
Marketing Status:  Discontinued
Patent and Exclusivity Information

PERMAX (PERGOLIDE MESYLATE)
EQ 0.25MG BASE
Marketing Status: Discontinued

Active Ingredient: PERGOLIDE MESYLATE
Proprietary Name: PERMAX
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 0.25MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N019385
Product Number: 002
Approval Date: Dec 30, 1988
Applicant Holder Full Name: VALEANT PHARMACEUTICALS INTERNATIONAL
Marketing Status:  Discontinued
Patent and Exclusivity Information

PERMAX (PERGOLIDE MESYLATE)
EQ 1MG BASE
Marketing Status: Discontinued

Active Ingredient: PERGOLIDE MESYLATE
Proprietary Name: PERMAX
Dosage Form; Route of Administration: TABLET; ORAL
Strength: EQ 1MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N019385
Product Number: 003
Approval Date: Dec 30, 1988
Applicant Holder Full Name: VALEANT PHARMACEUTICALS INTERNATIONAL
Marketing Status:  Discontinued
Patent and Exclusivity Information