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FDA NDA · NDA204914

LAMIVUDINE; ZIDOVUDINE

Sponsor: MYLAN LABS

APPLICATION
NDA204914
TYPE
NDA
LATEST ACTION
2015-05-14
ROUTE
ORAL SUSPENSION
DOSAGE FORM
TABLET
MARKETING STATUS
None (Tentative Approval)

Products

LAMIVUDINE; ZIDOVUDINENone (Tentative Approval)
LAMIVUDINE 30MG, ZIDOVUDINE 60MG · TABLET · ORAL SUSPENSION

Approval history

2015-05-14Manufacturing (CMC) · Supplement 1AP
2014-02-04Type 5 - New Formulation or New Manufacturer · Original · standardLetterTA
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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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