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FDA ANDA · ANDA207578

RANITIDINE HYDROCHLORIDE

Sponsor: AUROBINDO PHARMA

APPLICATION
ANDA207578
TYPE
ANDA
ORIGINAL APPROVAL
2017-11-13
LATEST ACTION
2017-11-13
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Discontinued

Products

RANITIDINE HYDROCHLORIDEDiscontinued
RANITIDINE HYDROCHLORIDE EQ 150MG BASE · TABLET · ORAL

Approval history

2017-11-13UNKNOWN · 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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