Drugs@FDA: FDA-Approved Drugs
New Drug Application (NDA): 012339
Company: SANOFI AVENTIS US
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 |