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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 090854
Company: TEVA PHARMS USA

Products on ANDA 090854

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	TE Code	RLD	RS
EPTIFIBATIDE	EPTIFIBATIDE	2MG/ML	INJECTABLE;INJECTION	Prescription	AP	No	No

Approval Date(s) and History, Letters, Labels, Reviews for ANDA 090854

Original Approvals or Tentative Approvals

Action Date	Submission	Action Type	Submission Classification	Review Priority; Orphan Status	Letters, Reviews, Labels, Patient Package Insert	Notes	Url
06/12/2015	ORIG-1	Approval				Label is not available on this site.

Therapeutic Equivalents for ANDA 090854

EPTIFIBATIDE

INJECTABLE;INJECTION; 2MG/ML
TE Code = AP

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	RLD	TE Code	Application No.	Company
EPTIFIBATIDE	EPTIFIBATIDE	2MG/ML	INJECTABLE;INJECTION	Prescription	No	AP	206127	EUGIA PHARMA
EPTIFIBATIDE	EPTIFIBATIDE	2MG/ML	INJECTABLE;INJECTION	Prescription	No	AP	213599	HONG KONG
EPTIFIBATIDE	EPTIFIBATIDE	2MG/ML	INJECTABLE;INJECTION	Prescription	No	AP	203258	MYLAN LABS LTD
EPTIFIBATIDE	EPTIFIBATIDE	2MG/ML	INJECTABLE;INJECTION	Prescription	No	AP	204693	SAGENT PHARMS INC
EPTIFIBATIDE	EPTIFIBATIDE	2MG/ML	INJECTABLE;INJECTION	Prescription	No	AP	213081	SHUANGCHENG
EPTIFIBATIDE	EPTIFIBATIDE	2MG/ML	INJECTABLE;INJECTION	Prescription	No	AP	209864	SLATE RUN PHARMA
EPTIFIBATIDE	EPTIFIBATIDE	2MG/ML	INJECTABLE;INJECTION	Prescription	No	AP	090854	TEVA PHARMS USA

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