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FDA ANDA · ANDA090679

LAMIVUDINE AND ZIDOVUDINE

Sponsor: MACLEODS PHARMS LTD

APPLICATION
ANDA090679
TYPE
ANDA
ORIGINAL APPROVAL
2018-08-29
LATEST ACTION
2019-12-13
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
Prescription

Products

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

Approval history

2019-12-13Labeling · Supplement 16 · standardAP
2018-08-29OriginalAP
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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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