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FDA ANDA · ANDA077601

CITALOPRAM HYDROBROMIDE

Sponsor: PHARM ASSOC

APPLICATION
ANDA077601
TYPE
ANDA
ORIGINAL APPROVAL
2005-11-15
LATEST ACTION
2023-08-18
ROUTE
ORAL
DOSAGE FORM
SOLUTION
MARKETING STATUS
Discontinued

Products

CITALOPRAM HYDROBROMIDEDiscontinued
CITALOPRAM HYDROBROMIDE EQ 10MG BASE/5ML · SOLUTION · ORAL

Approval history

2023-08-18Labeling · Supplement 9 · standardAP
2021-09-21Labeling · Supplement 8 · standardAP
2021-09-13Labeling · Supplement 7 · standardAP
2017-01-04Labeling · Supplement 6 · standardAP
2015-07-07Labeling · Supplement 5 · standardAP
2014-07-17Labeling · Supplement 4 · standardAP
2014-07-11Labeling · Supplement 3 · standardAP
2005-11-15OriginalOther Important Information from FDAAP
VIEW ON DRUGS@FDA ↗

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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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