Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 206358
Company: FDC LTD

Products on ANDA 206358

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	TE Code	RLD	RS
CEFIXIME	CEFIXIME	400MG	TABLET;ORAL	Prescription	None	No	Yes

Approval Date(s) and History, Letters, Labels, Reviews for ANDA 206358

Original Approvals or Tentative Approvals

Action Date	Submission	Action Type	Submission Classification	Review Priority; Orphan Status	Letters, Reviews, Labels, Patient Package Insert	Notes	Url
12/17/2024	ORIG-1	Approval		STANDARD		Label is not available on this site.