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Serving hundreds of leading biopharmaceutical companies globally:

US Army
Johnson and Johnson

Generated: June 24, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 070012

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NDA 070012 describes DOPAMINE HYDROCHLORIDE, which is a drug marketed by Abbott, Abraxis Pharm, Baxter Hlthcare, Hikma Intl Pharms, Hospira, Igi Labs Inc, Intl Medication, Luitpold, Lyphomed, Smith And Nephew, Teligent, Teva Parenteral, Warner Chilcott, and B Braun, and is included in thirty-six NDAs. It is available from seven suppliers. Additional details are available on the DOPAMINE HYDROCHLORIDE profile page.

The generic ingredient in DOPAMINE HYDROCHLORIDE is dopamine hydrochloride. There are nine drug master file entries for this compound. Eight suppliers are listed for this compound. Additional details are available on the dopamine hydrochloride profile page.
Summary for 070012
Applicant:Abraxis Pharm
Ingredient:dopamine hydrochloride
Formulation / Manufacturing:see details
Pharmacology for NDA: 070012
Mechanism of ActionOsmotic Activity
Physiological EffectIncreased Intravascular Volume
Medical Subject Heading (MeSH) Categories for 070012
Suppliers and Packaging for NDA: 070012
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
DOPAMINE HYDROCHLORIDE dopamine hydrochloride INJECTABLE;INJECTION 070012 NDA Hospira Inc. 0409-1029 N 0409-1029-01
DOPAMINE HYDROCHLORIDE dopamine hydrochloride INJECTABLE;INJECTION 070012 NDA Hospira Inc. 0409-1029 N 0409-1029-02

Profile for product number 001

Active Rx/OTC/Discontinued:DISCNDosage:INJECTABLE;INJECTIONStrength40MG/ML
Approval Date:Jun 12, 1985TE:RLD:No

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Serving hundreds of leading biopharmaceutical companies globally:

Harvard Business School
Queensland Health
Fish and Richardson

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