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FDA ANDA · ANDA079081

LAMIVUDINE AND ZIDOVUDINE

Sponsor: CHARTWELL RX

APPLICATION
ANDA079081
TYPE
ANDA
ORIGINAL APPROVAL
2011-05-25
LATEST ACTION
2015-08-13
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Discontinued

Products

LAMIVUDINE AND ZIDOVUDINEDiscontinued
LAMIVUDINE 150MG, ZIDOVUDINE 300MG · TABLET · ORAL

Approval history

2015-08-13Labeling · Supplement 2AP
2011-05-25OriginalAP
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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