Product Details for NDA 019005
BRETYLIUM TOSYLATE IN DEXTROSE 5% (BRETYLIUM TOSYLATE)
200MG/100ML
Marketing Status: Discontinued
400MG/100ML
Marketing Status: Discontinued
800MG/100ML
Marketing Status: Discontinued
200MG/100ML
Marketing Status: Discontinued
Active Ingredient: BRETYLIUM TOSYLATE
Proprietary Name: BRETYLIUM TOSYLATE IN DEXTROSE 5%
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 200MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N019005
Product Number: 002
Approval Date: Apr 29, 1986
Applicant Holder Full Name: ABBOTT LABORATORIES PHARMACEUTICAL PRODUCTS DIV
Marketing Status: Discontinued
Patent and Exclusivity Information
BRETYLIUM TOSYLATE IN DEXTROSE 5% (BRETYLIUM TOSYLATE)
Proprietary Name: BRETYLIUM TOSYLATE IN DEXTROSE 5%
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 200MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N019005
Product Number: 002
Approval Date: Apr 29, 1986
Applicant Holder Full Name: ABBOTT LABORATORIES PHARMACEUTICAL PRODUCTS DIV
Marketing Status: Discontinued
Patent and Exclusivity Information
400MG/100ML
Marketing Status: Discontinued
Active Ingredient: BRETYLIUM TOSYLATE
Proprietary Name: BRETYLIUM TOSYLATE IN DEXTROSE 5%
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 400MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N019005
Product Number: 003
Approval Date: Apr 29, 1986
Applicant Holder Full Name: ABBOTT LABORATORIES PHARMACEUTICAL PRODUCTS DIV
Marketing Status: Discontinued
Patent and Exclusivity Information
BRETYLIUM TOSYLATE IN DEXTROSE 5% (BRETYLIUM TOSYLATE)
Proprietary Name: BRETYLIUM TOSYLATE IN DEXTROSE 5%
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 400MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N019005
Product Number: 003
Approval Date: Apr 29, 1986
Applicant Holder Full Name: ABBOTT LABORATORIES PHARMACEUTICAL PRODUCTS DIV
Marketing Status: Discontinued
Patent and Exclusivity Information
800MG/100ML
Marketing Status: Discontinued
Active Ingredient: BRETYLIUM TOSYLATE
Proprietary Name: BRETYLIUM TOSYLATE IN DEXTROSE 5%
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 800MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N019005
Product Number: 001
Approval Date: Apr 29, 1986
Applicant Holder Full Name: ABBOTT LABORATORIES PHARMACEUTICAL PRODUCTS DIV
Marketing Status: Discontinued
Patent and Exclusivity Information
Proprietary Name: BRETYLIUM TOSYLATE IN DEXTROSE 5%
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 800MG/100ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N019005
Product Number: 001
Approval Date: Apr 29, 1986
Applicant Holder Full Name: ABBOTT LABORATORIES PHARMACEUTICAL PRODUCTS DIV
Marketing Status: Discontinued
Patent and Exclusivity Information