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FDA ANDA · ANDA078484

GALANTAMINE HYDROBROMIDE

Sponsor: IMPAX LABS

APPLICATION
ANDA078484
TYPE
ANDA
ORIGINAL APPROVAL
2009-05-27
LATEST ACTION
2023-06-28
ROUTE
ORAL
DOSAGE FORM
CAPSULE, EXTENDED RELEASE
MARKETING STATUS
Discontinued

Products

GALANTAMINE HYDROBROMIDEDiscontinued
GALANTAMINE HYDROBROMIDE EQ 24MG BASE · CAPSULE, EXTENDED RELEASE · ORAL
GALANTAMINE HYDROBROMIDEDiscontinued
GALANTAMINE HYDROBROMIDE EQ 8MG BASE · CAPSULE, EXTENDED RELEASE · ORAL
GALANTAMINE HYDROBROMIDEDiscontinued
GALANTAMINE HYDROBROMIDE EQ 16MG BASE · CAPSULE, EXTENDED RELEASE · ORAL

Approval history

2023-06-28Labeling · Supplement 11 · standardAP
2023-06-28Labeling · Supplement 10 · standardAP
2019-12-06Labeling · Supplement 8 · standardAP
2009-05-27OriginalAP
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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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