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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 074121
Company: PHARMOBEDIENT
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
NAPROXEN NAPROXEN 250MG TABLET;ORAL Discontinued None No No
NAPROXEN NAPROXEN 375MG TABLET;ORAL Discontinued None No No
NAPROXEN NAPROXEN 500MG TABLET;ORAL Discontinued None No No
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