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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 070649
Company: ABRAXIS PHARM

Products on ANDA 070649

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	TE Code	RLD	RS
NALOXONE HYDROCHLORIDE	NALOXONE HYDROCHLORIDE	0.4MG/ML	INJECTABLE;INJECTION	Discontinued	None	No	No

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