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FDA ANDA · ANDA071071

HALOPERIDOL

Sponsor: PUREPAC PHARM

APPLICATION
ANDA071071
TYPE
ANDA
ORIGINAL APPROVAL
1986-11-03
LATEST ACTION
1998-02-20
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Discontinued

Products

HALOPERIDOLDiscontinued
HALOPERIDOL 0.5MG · TABLET · ORAL

Approval history

1998-02-20Labeling · Supplement 4AP
1991-05-09Labeling · Supplement 9AP
1989-04-19Labeling · Supplement 8AP
1986-11-03OriginalAP
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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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