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FDA ANDA · ANDA205407

CITALOPRAM HYDROBROMIDE

Sponsor: JUBILANT GENERICS

APPLICATION
ANDA205407
TYPE
ANDA
ORIGINAL APPROVAL
2015-12-23
LATEST ACTION
2024-11-14
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Discontinued

Products

CITALOPRAM HYDROBROMIDEDiscontinued
CITALOPRAM HYDROBROMIDE EQ 40MG BASE · TABLET · ORAL
CITALOPRAM HYDROBROMIDEDiscontinued
CITALOPRAM HYDROBROMIDE EQ 10MG BASE · TABLET · ORAL
CITALOPRAM HYDROBROMIDEDiscontinued
CITALOPRAM HYDROBROMIDE EQ 20MG BASE · TABLET · ORAL

Approval history

2024-11-14Labeling · Supplement 9 · standardAP
2024-11-14Labeling · Supplement 1 · standardAP
2024-11-14Labeling · Supplement 6 · standardAP
2015-12-23UNKNOWN · Original · standardAP
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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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