OXYCODONE HYDROCHLORIDE (OXYCODONE HYDROCHLORIDE) — FDA Approval ANDA202160 (AUROLIFE PHARMA LLC)
OXYCODONE HYDROCHLORIDE (OXYCODONE HYDROCHLORIDE) — FDA Approval ANDA202160 (AUROLIFE PHARMA LLC) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: OXYCODONE HYDROCHLORIDE; Active ingredients: OXYCODONE HYDROCHLORIDE; Application number: ANDA202160.
| Brand name | OXYCODONE HYDROCHLORIDE |
|---|---|
| Active ingredients | OXYCODONE HYDROCHLORIDE |
| Application number | ANDA202160 |
| Sponsor | AUROLIFE PHARMA LLC |
| Dosage form | TABLET |
| Route | ORAL |
| Marketing status | Prescription |
| Products in application | 3 |
| First approval date | 20121119 |
| Source | openFDA Drugs@FDA |
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