NOVAFED (PSEUDOEPHEDRINE HYDROCHLORIDE) — FDA Approval NDA017603 (SANOFI AVENTIS US)
NOVAFED (PSEUDOEPHEDRINE HYDROCHLORIDE) — FDA Approval NDA017603 (SANOFI AVENTIS US) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: NOVAFED; Active ingredients: PSEUDOEPHEDRINE HYDROCHLORIDE; Application number: NDA017603.
| Brand name | NOVAFED |
|---|---|
| Active ingredients | PSEUDOEPHEDRINE HYDROCHLORIDE |
| Application number | NDA017603 |
| Sponsor | SANOFI AVENTIS US |
| Dosage form | CAPSULE, EXTENDED RELEASE |
| Route | ORAL |
| Marketing status | Discontinued |
| Products in application | 1 |
| First approval date | 19750829 |
| Source | openFDA Drugs@FDA |
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