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Drugs@FDA: FDA-Approved Drugs

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New Drug Application (NDA): 018197
Company: BASF

Products on NDA 18197

Drug Name	Active Ingredients	Strength	Dosage Form/Route	Marketing Status	TE Code	RLD	RS
IBU	IBUPROFEN	400MG	TABLET;ORAL	Discontinued	None	No	No
RUFEN	IBUPROFEN	600MG	TABLET;ORAL	Discontinued	None	No	No

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