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FDA NDA · NDA202157

LAMIVUDINE; NEVIRAPINE; ZIDOVUDINE

Sponsor: HETERO LABS UNIT III

APPLICATION
NDA202157
TYPE
NDA
ROUTE
ORAL
DOSAGE FORM
TABLET
MARKETING STATUS
None (Tentative Approval)

Products

LAMIVUDINE; NEVIRAPINE; ZIDOVUDINENone (Tentative Approval)
LAMIVUDINE 150MG, NEVIRAPINE 200MG, ZIDOVUDINE 300MG · TABLET · ORAL

Approval history

2011-11-18Type 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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