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Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

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Product Details for NDA 019099

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DOPAMINE HYDROCHLORIDE AND DEXTROSE 5% (DOPAMINE HYDROCHLORIDE)
80MG/100ML
Marketing Status: Discontinued
Active Ingredient: DOPAMINE HYDROCHLORIDE
Proprietary Name: DOPAMINE HYDROCHLORIDE AND DEXTROSE 5%
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 80MG/100ML
Reference Listed Drug: Yes
Reference Standard: No
TE Code: 
Application Number: N019099
Product Number: 002
Approval Date: Oct 15, 1986
Applicant Holder Full Name: B BRAUN MEDICAL INC
Marketing Status:  Discontinued
Patent and Exclusivity Information
DOPAMINE HYDROCHLORIDE AND DEXTROSE 5% (DOPAMINE HYDROCHLORIDE)
320MG/100ML
Marketing Status: Discontinued
Active Ingredient: DOPAMINE HYDROCHLORIDE
Proprietary Name: DOPAMINE HYDROCHLORIDE AND DEXTROSE 5%
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 320MG/100ML
Reference Listed Drug: Yes
Reference Standard: No
TE Code: 
Application Number: N019099
Product Number: 004
Approval Date: Oct 15, 1986
Applicant Holder Full Name: B BRAUN MEDICAL INC
Marketing Status:  Discontinued
Patent and Exclusivity Information
DOPAMINE HYDROCHLORIDE AND DEXTROSE 5% IN PLASTIC CONTAINER (DOPAMINE HYDROCHLORIDE)
40MG/100ML
Marketing Status: Discontinued
Active Ingredient: DOPAMINE HYDROCHLORIDE
Proprietary Name: DOPAMINE HYDROCHLORIDE AND DEXTROSE 5% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 40MG/100ML
Reference Listed Drug: Yes
Reference Standard: No
TE Code: 
Application Number: N019099
Product Number: 001
Approval Date: Oct 15, 1986
Applicant Holder Full Name: B BRAUN MEDICAL INC
Marketing Status:  Discontinued
Patent and Exclusivity Information
DOPAMINE HYDROCHLORIDE AND DEXTROSE 5% IN PLASTIC CONTAINER (DOPAMINE HYDROCHLORIDE)
160MG/100ML
Marketing Status: Discontinued
Active Ingredient: DOPAMINE HYDROCHLORIDE
Proprietary Name: DOPAMINE HYDROCHLORIDE AND DEXTROSE 5% IN PLASTIC CONTAINER
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 160MG/100ML
Reference Listed Drug: Yes
Reference Standard: No
TE Code: 
Application Number: N019099
Product Number: 003
Approval Date: Oct 15, 1986
Applicant Holder Full Name: B BRAUN MEDICAL INC
Marketing Status:  Discontinued
Patent and Exclusivity Information
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