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FDA ANDA · ANDA212001

GANCICLOVIR SODIUM

Sponsor: CUSTOPHARM INC

APPLICATION
ANDA212001
TYPE
ANDA
ORIGINAL APPROVAL
2019-06-20
LATEST ACTION
2019-06-20
ROUTE
INJECTION
DOSAGE FORM
INJECTABLE
MARKETING STATUS
Discontinued

Products

GANCICLOVIR SODIUMDiscontinued
GANCICLOVIR SODIUM EQ 500MG BASE/VIAL · INJECTABLE · INJECTION

Approval history

2019-06-20UNKNOWN · Original · standardAP
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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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