Drugs@FDA: FDA-Approved Drugs

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New Drug Application (NDA): 012339
Company: SANOFI AVENTIS US
Drug Name Active Ingredients Strength Dosage Form/Route Marketing Status TE Code RLD RS
BRONKOMETER ISOETHARINE MESYLATE 0.34MG/INH AEROSOL, METERED;INHALATION Discontinued None No No
BRONKOSOL ISOETHARINE HYDROCHLORIDE 1% SOLUTION;INHALATION Discontinued None No No
BRONKOSOL ISOETHARINE HYDROCHLORIDE 0.25% SOLUTION;INHALATION Discontinued None No No

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