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Serving hundreds of leading biopharmaceutical companies globally:

Cantor Fitzgerald
Federal Trade Commission
Express Scripts
Johnson and Johnson
Queensland Health

Generated: June 21, 2018

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 070799

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NDA 070799 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 070799
Ingredient:dopamine hydrochloride
Formulation / Manufacturing:see details
Pharmacology for NDA: 070799
Medical Subject Heading (MeSH) Categories for 070799
Suppliers and Packaging for NDA: 070799
Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
DOPAMINE HYDROCHLORIDE dopamine hydrochloride INJECTABLE;INJECTION 070799 ANDA American Regent, Inc. 0517-1805 N 0517-1805-25
DOPAMINE HYDROCHLORIDE dopamine hydrochloride INJECTABLE;INJECTION 070799 ANDA Cardinal Health 55154-5712 N 55154-5712-5

Profile for product number 001

Active Rx/OTC/Discontinued:RXDosage:INJECTABLE;INJECTIONStrength40MG/ML
Approval Date:Feb 11, 1987TE:APRLD:No

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Serving hundreds of leading biopharmaceutical companies globally:

Farmers Insurance
Express Scripts

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