NALOXONE (NALOXONE HYDROCHLORIDE) — FDA Approval ANDA070496 (HIKMA)
NALOXONE (NALOXONE HYDROCHLORIDE) — FDA Approval ANDA070496 (HIKMA) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: NALOXONE; Active ingredients: NALOXONE HYDROCHLORIDE; Application number: ANDA070496.
| Brand name | NALOXONE |
|---|---|
| Active ingredients | NALOXONE HYDROCHLORIDE |
| Application number | ANDA070496 |
| Sponsor | HIKMA |
| Dosage form | INJECTABLE |
| Route | INJECTION |
| Marketing status | Discontinued |
| Products in application | 1 |
| First approval date | 19851022 |
| Source | openFDA Drugs@FDA |
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