Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 216805
Company: ZHEJIANG POLY PHARM

Products on ANDA 216805

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	TE Code	RLD	RS
VORICONAZOLE	VORICONAZOLE	200MG/5ML	FOR SUSPENSION;ORAL	Prescription	AB	No	No

Approval Date(s) and History, Letters, Labels, Reviews for ANDA 216805

Original Approvals or Tentative Approvals

Action Date	Submission	Action Type	Submission Classification	Review Priority; Orphan Status	Letters, Reviews, Labels, Patient Package Insert	Notes	Url
01/02/2024	ORIG-1	Approval		STANDARD		Label is not available on this site.

Supplements

Action Date	Submission	Supplement Categories or Approval Type	Letters, Reviews, Labels, Patient Package Insert	Note	Url
08/25/2025	SUPPL-1	Labeling-Package Insert		Label is not available on this site.

Therapeutic Equivalents for ANDA 216805

VORICONAZOLE

FOR SUSPENSION;ORAL; 200MG/5ML
TE Code = AB

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	RLD	TE Code	Application No.	Company
VFEND	VORICONAZOLE	200MG/5ML	FOR SUSPENSION;ORAL	Prescription	Yes	AB	021630	PF PRISM CV
VORICONAZOLE	VORICONAZOLE	200MG/5ML	FOR SUSPENSION;ORAL	Prescription	No	AB	205034	AMNEAL PHARMS
VORICONAZOLE	VORICONAZOLE	200MG/5ML	FOR SUSPENSION;ORAL	Prescription	No	AB	211598	HETERO LABS LTD V
VORICONAZOLE	VORICONAZOLE	200MG/5ML	FOR SUSPENSION;ORAL	Prescription	No	AB	206799	NOVEL LABS INC
VORICONAZOLE	VORICONAZOLE	200MG/5ML	FOR SUSPENSION;ORAL	Prescription	No	AB	216805	ZHEJIANG POLY PHARM