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Drugs@FDA: FDA-Approved Drugs

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New Drug Application (NDA): 019228
Company: ABRAXIS PHARM

Products on NDA 19228

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	TE Code	RLD	RS
MANGANESE SULFATE	MANGANESE SULFATE	EQ 0.1MG MANGANESE/ML Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	INJECTABLE;INJECTION	Discontinued	None	Yes	No

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