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Details for New Drug Application (NDA): 074279

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NDA 074279 describes DOBUTAMINE HYDROCHLORIDE, which is a drug marketed by Teva Parenteral, Watson Labs, Hospira, Luitpold, West-ward Pharms Int, Watson Labs Inc, Baxter Hlthcare, and Teligent Pharma Inc, and is included in fourteen NDAs. It is available from three suppliers. Additional details are available on the DOBUTAMINE HYDROCHLORIDE profile page.

The generic ingredient in DOBUTAMINE HYDROCHLORIDE is dobutamine hydrochloride. There are fourteen drug master file entries for this compound. Four suppliers are listed for this compound. Additional details are available on the dobutamine hydrochloride profile page.

Summary for NDA: 074279

Tradename:
DOBUTAMINE HYDROCHLORIDE
Applicant:
Watson Labs Inc
Ingredient:
dobutamine hydrochloride
Patents:0
Formulation / Manufacturing:see details

Summary for product number 001

Active Rx/OTC/Discontinued:DISCNDosage:INJECTABLE;INJECTIONStrengthEQ 12.5MG BASE/ML
Approval Date:Feb 18, 1998TE: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.

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