BRONKOSOL (ISOETHARINE HYDROCHLORIDE) — FDA Approval NDA012339 (SANOFI AVENTIS US)
BRONKOSOL (ISOETHARINE HYDROCHLORIDE) — FDA Approval NDA012339 (SANOFI AVENTIS US) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: BRONKOSOL; Active ingredients: ISOETHARINE HYDROCHLORIDE; Application number: NDA012339.
| Brand name | BRONKOSOL |
|---|---|
| Active ingredients | ISOETHARINE HYDROCHLORIDE |
| Application number | NDA012339 |
| Sponsor | SANOFI AVENTIS US |
| Dosage form | SOLUTION |
| Route | INHALATION |
| Marketing status | Discontinued |
| Products in application | 3 |
| Source | openFDA Drugs@FDA |
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