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FDA ANDA · ANDA074885

ACYCLOVIR IN SODIUM CHLORIDE 0.9% PRESERVATIVE FREE

Sponsor: EUROHLTH INTL SARL

APPLICATION
ANDA074885
TYPE
ANDA
ORIGINAL APPROVAL
1997-12-19
LATEST ACTION
2000-04-19
ROUTE
INJECTION
DOSAGE FORM
INJECTABLE
MARKETING STATUS
Discontinued

Products

ACYCLOVIR IN SODIUM CHLORIDE 0.9% PRESERVATIVE FREEDiscontinued
ACYCLOVIR SODIUM EQ 1GM BASE/VIAL · INJECTABLE · INJECTION
ACYCLOVIR IN SODIUM CHLORIDE 0.9% PRESERVATIVE FREEDiscontinued
ACYCLOVIR SODIUM EQ 500MG BASE/VIAL · INJECTABLE · INJECTION

Approval history

2000-04-19Labeling · Supplement 1AP
1997-12-19OriginalAP
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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