NALOXONE (NALOXONE HYDROCHLORIDE) — FDA Approval ANDA070191 (WYETH AYERST)
NALOXONE (NALOXONE HYDROCHLORIDE) — FDA Approval ANDA070191 (WYETH AYERST) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: NALOXONE; Active ingredients: NALOXONE HYDROCHLORIDE; Application number: ANDA070191.
| Brand name | NALOXONE |
|---|---|
| Active ingredients | NALOXONE HYDROCHLORIDE |
| Application number | ANDA070191 |
| Sponsor | WYETH AYERST |
| Dosage form | INJECTABLE |
| Route | INJECTION |
| Marketing status | Discontinued |
| Products in application | 1 |
| First approval date | 19851002 |
| Source | openFDA Drugs@FDA |
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