OXYMORPHONE HYDROCHLORIDE (OXYMORPHONE HYDROCHLORIDE) — FDA Approval ANDA200822 (HIKMA)
OXYMORPHONE HYDROCHLORIDE (OXYMORPHONE HYDROCHLORIDE) — FDA Approval ANDA200822 (HIKMA) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: OXYMORPHONE HYDROCHLORIDE; Active ingredients: OXYMORPHONE HYDROCHLORIDE; Application number: ANDA200822.
| Brand name | OXYMORPHONE HYDROCHLORIDE |
|---|---|
| Active ingredients | OXYMORPHONE HYDROCHLORIDE |
| Application number | ANDA200822 |
| Sponsor | HIKMA |
| Dosage form | TABLET, EXTENDED RELEASE |
| Route | ORAL |
| Marketing status | Discontinued |
| Products in application | 7 |
| First approval date | 20130715 |
| Source | openFDA Drugs@FDA |
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