U.S. flag An official website of the United States government

U.S. Food and Drug Administration
  1. Home
  2. Drug Databases
  3. Orange Book Home

Orange Book: Approved Drug Products with Therapeutic Equivalence Evaluations

Home | Back to Search Results

Product Details for NDA 018132

Expand all

DOPAMINE HYDROCHLORIDE (DOPAMINE HYDROCHLORIDE)
40MG/ML
Marketing Status: Prescription
Active Ingredient: DOPAMINE HYDROCHLORIDE
Proprietary Name: DOPAMINE HYDROCHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 40MG/ML
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AP
Application Number: N018132
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: HOSPIRA INC
Marketing Status:  Prescription
Patent and Exclusivity Information
DOPAMINE HYDROCHLORIDE (DOPAMINE HYDROCHLORIDE)
80MG/100ML
Marketing Status: Prescription
Active Ingredient: DOPAMINE HYDROCHLORIDE
Proprietary Name: DOPAMINE HYDROCHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 80MG/100ML
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AP
Application Number: N018132
Product Number: 002
Approval Date: Feb 4, 1982
Applicant Holder Full Name: HOSPIRA INC
Marketing Status:  Prescription
Patent and Exclusivity Information
DOPAMINE HYDROCHLORIDE (DOPAMINE HYDROCHLORIDE)
80MG/ML
Marketing Status: Prescription
Active Ingredient: DOPAMINE HYDROCHLORIDE
Proprietary Name: DOPAMINE HYDROCHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 80MG/ML
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AP
Application Number: N018132
Product Number: 004
Approval Date: Jul 9, 1982
Applicant Holder Full Name: HOSPIRA INC
Marketing Status:  Prescription
Patent and Exclusivity Information
DOPAMINE HYDROCHLORIDE (DOPAMINE HYDROCHLORIDE)
160MG/100ML
Marketing Status: Prescription
Active Ingredient: DOPAMINE HYDROCHLORIDE
Proprietary Name: DOPAMINE HYDROCHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 160MG/100ML
Reference Listed Drug: Yes
Reference Standard: Yes
TE Code: AP
Application Number: N018132
Product Number: 003
Approval Date: Feb 4, 1982
Applicant Holder Full Name: HOSPIRA INC
Marketing Status:  Prescription
Patent and Exclusivity Information
Back to Top