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FDA ANDA · ANDA202058

ZIDOVUDINE

Sponsor: HEC PHARM

APPLICATION
ANDA202058
TYPE
ANDA
ORIGINAL APPROVAL
2011-10-07
LATEST ACTION
2020-01-22
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Discontinued

Products

ZIDOVUDINEDiscontinued
ZIDOVUDINE 300MG · TABLET · ORAL

Approval history

2020-01-22Labeling · Supplement 14 · standardAP
2020-01-22Labeling · Supplement 9 · standardAP
2013-06-03Labeling · Supplement 3 · standardAP
2013-02-01Labeling · Supplement 2 · standardAP
2011-10-07UNKNOWN · OriginalLetterAP
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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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