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FDA ANDA · ANDA204520

GEMCITABINE HYDROCHLORIDE

Sponsor: GLAND

APPLICATION
ANDA204520
TYPE
ANDA
ORIGINAL APPROVAL
2016-01-05
LATEST ACTION
2024-09-24
ROUTE
INTRAVENOUS, INJECTION
DOSAGE FORM
INJECTABLE
MARKETING STATUS
Prescription

Products

GEMCITABINE HYDROCHLORIDEPrescription
GEMCITABINE HYDROCHLORIDE EQ 1GM BASE/VIAL · INJECTABLE · INJECTION
GEMCITABINE HYDROCHLORIDEPrescription
GEMCITABINE HYDROCHLORIDE EQ 200MG BASE/VIAL · INJECTABLE · INJECTION

Approval history

2024-09-24Labeling · Supplement 11 · standardAP
2019-10-03Labeling · Supplement 6 · standardAP
2019-10-03Labeling · Supplement 4 · standardAP
2019-10-03Labeling · Supplement 3 · standardAP
2016-01-05UNKNOWN · OriginalAP
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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