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Serving leading biopharmaceutical companies globally:

Queensland Health
Federal Trade Commission
Cantor Fitzgerald

Generated: December 16, 2017

DrugPatentWatch Database Preview

Details for New Drug Application (NDA): 070820

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NDA 070820 describes DOPAMINE HYDROCHLORIDE, which is a drug marketed by Abbott, Abraxis Pharm, Baxter Hlthcare, Hospira, Igi Labs Inc, Intl Medication, Luitpold, Lyphomed, Smith And Nephew, Teligent, Teva Parenteral, Warner Chilcott, and B Braun, and is included in thirty-five NDAs. It is available from six 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. Seven suppliers are listed for this compound. Additional details are available on the dopamine hydrochloride profile page.

Summary for 070820

Formulation / Manufacturing:see details

Pharmacology for NDA: 070820


Medical Subject Heading (MeSH) Categories for 070820

Suppliers and Packaging for NDA: 070820

Tradename Generic Name Dosage NDA Application Type Supplier National Drug Code Package Code Package
DOPAMINE HYDROCHLORIDE dopamine hydrochloride INJECTABLE;INJECTION 070820 ANDA American Regent, Inc. 0517-1905 0517-1905-25 25 VIAL, SINGLE-DOSE in 1 BOX (0517-1905-25) > 5 mL in 1 VIAL, SINGLE-DOSE
DOPAMINE HYDROCHLORIDE dopamine hydrochloride INJECTABLE;INJECTION 070820 ANDA Cardinal Health 55154-5708 55154-5708-8 1 VIAL, SINGLE-DOSE in 1 BAG (55154-5708-8) > 5 mL in 1 VIAL, SINGLE-DOSE

Summary for product number 001

Active Rx/OTC/Discontinued:RXDosage:INJECTABLE;INJECTIONStrength80MG/ML
Approval Date:Feb 11, 1987TE:APRLD:No

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Serving leading biopharmaceutical companies globally:

Harvard Business School
Chinese Patent Office
Johnson and Johnson
Queensland Health
Express Scripts

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