Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 019753

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ETHMOZINE (MORICIZINE HYDROCHLORIDE)
200MG
Marketing Status: Discontinued

Active Ingredient: MORICIZINE HYDROCHLORIDE
Proprietary Name: ETHMOZINE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 200MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N019753
Product Number: 001
Approval Date: Jun 19, 1990
Applicant Holder Full Name: SHIRE DEVELOPMENT INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

ETHMOZINE (MORICIZINE HYDROCHLORIDE)
250MG
Marketing Status: Discontinued

Active Ingredient: MORICIZINE HYDROCHLORIDE
Proprietary Name: ETHMOZINE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 250MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N019753
Product Number: 002
Approval Date: Jun 19, 1990
Applicant Holder Full Name: SHIRE DEVELOPMENT INC
Marketing Status:  Discontinued
Patent and Exclusivity Information

ETHMOZINE (MORICIZINE HYDROCHLORIDE)
300MG
Marketing Status: Discontinued

Active Ingredient: MORICIZINE HYDROCHLORIDE
Proprietary Name: ETHMOZINE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 300MG
Reference Listed Drug: No
Reference Standard: No
TE Code: 
Application Number: N019753
Product Number: 003
Approval Date: Jun 19, 1990
Applicant Holder Full Name: SHIRE DEVELOPMENT INC
Marketing Status:  Discontinued
Patent and Exclusivity Information