Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 009078

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PARSIDOL (ETHOPROPAZINE HYDROCHLORIDE)
10MG
Marketing Status: Discontinued

Active Ingredient: ETHOPROPAZINE HYDROCHLORIDE
Proprietary Name: PARSIDOL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 10MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N009078
Product Number: 003
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

PARSIDOL (ETHOPROPAZINE HYDROCHLORIDE)
50MG
Marketing Status: Discontinued

Active Ingredient: ETHOPROPAZINE HYDROCHLORIDE
Proprietary Name: PARSIDOL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 50MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N009078
Product Number: 006
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

PARSIDOL (ETHOPROPAZINE HYDROCHLORIDE)
100MG
Marketing Status: Discontinued

Active Ingredient: ETHOPROPAZINE HYDROCHLORIDE
Proprietary Name: PARSIDOL
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 100MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N009078
Product Number: 008
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