Active Ingredient: THIORIDAZINE HYDROCHLORIDE
Proprietary Name: THIORIDAZINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 10MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A089953
Product Number: 004
Approval Date: Aug 1, 1986
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
Active Ingredient: THIORIDAZINE HYDROCHLORIDE
Proprietary Name: THIORIDAZINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 25MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A089953
Product Number: 003
Approval Date: Aug 1, 1986
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
Active Ingredient: THIORIDAZINE HYDROCHLORIDE
Proprietary Name: THIORIDAZINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 50MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A089953
Product Number: 002
Approval Date: Aug 1, 1986
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
Active Ingredient: THIORIDAZINE HYDROCHLORIDE
Proprietary Name: THIORIDAZINE HYDROCHLORIDE
Dosage Form; Route of Administration: TABLET; ORAL
Strength: 100MG
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A089953
Product Number: 001
Approval Date: Oct 7, 1988
Applicant Holder Full Name: SUN PHARMACEUTICAL INDUSTRIES INC
Marketing Status:
Discontinued
Patent and Exclusivity Information