APPLICATION
ANDA071812
TYPE
ANDA
ORIGINAL APPROVAL
1987-12-22
LATEST ACTION
1998-02-23
ROUTE
INJECTION
DOSAGE FORM
INJECTABLE
MARKETING STATUS
Discontinued
Products
METHYLDOPATE HYDROCHLORIDEDiscontinued
METHYLDOPATE HYDROCHLORIDE 50MG/ML · INJECTABLE · INJECTION
Approval history
1998-02-23Labeling · Supplement 7AP
1990-03-27Labeling · Supplement 5AP
1987-12-22OriginalAP
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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