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Drugs@FDA: FDA-Approved Drugs

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Abbreviated New Drug Application (ANDA): 088791
Company: NOVARTIS

Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
VASOCIDIN PREDNISOLONE ACETATE; SULFACETAMIDE SODIUM 0.5%;10% OINTMENT;OPHTHALMIC Discontinued None No No
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