KERLEDEX (BETAXOLOL HYDROCHLORIDE; CHLORTHALIDONE) — FDA Approval NDA019807 (SANOFI AVENTIS US)
KERLEDEX (BETAXOLOL HYDROCHLORIDE; CHLORTHALIDONE) — FDA Approval NDA019807 (SANOFI AVENTIS US) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: KERLEDEX; Active ingredients: BETAXOLOL HYDROCHLORIDE; CHLORTHALIDONE; Application number: NDA019807.
| Brand name | KERLEDEX |
|---|---|
| Active ingredients | BETAXOLOL HYDROCHLORIDE; CHLORTHALIDONE |
| Application number | NDA019807 |
| Sponsor | SANOFI AVENTIS US |
| Dosage form | TABLET |
| Route | ORAL |
| Marketing status | Discontinued |
| Products in application | 2 |
| First approval date | 19921030 |
| Source | openFDA Drugs@FDA |
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