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FDA ANDA · ANDA078460

GEMCITABINE

Sponsor: EUROHLTH INTL

APPLICATION
ANDA078460
TYPE
ANDA
ROUTE
INJECTION
DOSAGE FORM
INJECTABLE
MARKETING STATUS
None (Tentative Approval)

Products

GEMCITABINENone (Tentative Approval)
GEMCITABINE 200MG · INJECTABLE · INJECTION

Approval history

2010-01-19OriginalTA
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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