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Details for New Drug Application (NDA): 073000

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NDA 073000 describes DOPAMINE HYDROCHLORIDE, which is a drug marketed by Teva Parenteral, Hospira, Smith And Nephew, Abraxis Pharm, Intl Medication, Luitpold, Warner Chilcott, Lyphomed, Abbott, Igi Labs Inc, Baxter Hlthcare, and B Braun, and is included in thirty-five 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 NDA: 073000

Teva Parenteral
dopamine hydrochloride

Summary for product number 001

Active Rx/OTC/Discontinued:DISCNDosage:INJECTABLE;INJECTIONStrength80MG/ML
Approval Date:Oct 23, 1991TE:RLD:No

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Drugs may be covered by multiple patents or regulatory protections. All trademarks and applicant names are the property of their respective owners or licensors. Although great care is taken in the proper and correct provision of this service, thinkBiotech LLC does not accept any responsibility for possible consequences of errors or omissions in the provided data. The data presented herein is for information purposes only. There is no warranty that the data contained herein is error free. thinkBiotech performs no independent verifification of facts as provided by public sources nor are attempts made to provide legal or investing advice. Any reliance on data provided herein is done solely at the discretion of the user. Users of this service are advised to seek professional advice and independent confirmation before considering acting on any of the provided information. thinkBiotech LLC reserves the right to amend, extend or withdraw any part or all of the offered service without notice.