APPLICATION
ANDA072999
TYPE
ANDA
ORIGINAL APPROVAL
1991-10-23
LATEST ACTION
2001-06-21
ROUTE
INJECTION
DOSAGE FORM
INJECTABLE
MARKETING STATUS
Discontinued
Products
DOPAMINE HYDROCHLORIDEDiscontinued
DOPAMINE HYDROCHLORIDE 40MG/ML · INJECTABLE · INJECTION
Approval history
2001-06-21Labeling · Supplement 3AP
1998-04-23Labeling · Supplement 2AP
1997-09-09Labeling · Supplement 1AP
1991-10-23OriginalAP
Source: FDA Drugs@FDA. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data, not medical, legal, or regulatory advice.
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