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FDA ANDA · ANDA202774

BUPROPION HYDROCHLORIDE

Sponsor: JUBILANT GENERICS

APPLICATION
ANDA202774
TYPE
ANDA
ORIGINAL APPROVAL
2013-10-11
LATEST ACTION
2014-11-20
ROUTE
ORAL
DOSAGE FORM
TABLET, EXTENDED RELEASE
MARKETING STATUS
Discontinued

Products

BUPROPION HYDROCHLORIDEDiscontinued
BUPROPION HYDROCHLORIDE 200MG · TABLET, EXTENDED RELEASE · ORAL
BUPROPION HYDROCHLORIDEDiscontinued
BUPROPION HYDROCHLORIDE 100MG · TABLET, EXTENDED RELEASE · ORAL
BUPROPION HYDROCHLORIDEDiscontinued
BUPROPION HYDROCHLORIDE 150MG · TABLET, EXTENDED RELEASE · ORAL

Approval history

2014-11-20Labeling · Supplement 3 · standardAP
2014-11-20Labeling · Supplement 1 · standardAP
2013-10-11UNKNOWN · OriginalAP
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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