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FDA ANDA · ANDA202947

CABERGOLINE

Sponsor: PHARMOBEDIENT

APPLICATION
ANDA202947
TYPE
ANDA
ORIGINAL APPROVAL
2013-12-02
LATEST ACTION
2023-05-01
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Discontinued

Products

CABERGOLINEDiscontinued
CABERGOLINE 0.5MG · TABLET · ORAL

Approval history

2023-05-01Labeling · Supplement 2 · standardAP
2019-12-13Labeling · Supplement 1 · standardAP
2013-12-02UNKNOWN · OriginalAP
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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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