OXYCODONE AND ACETAMINOPHEN (ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE) — FDA Approval ANDA040800 (ACTAVIS ELIZABETH)
OXYCODONE AND ACETAMINOPHEN (ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE) — FDA Approval ANDA040800 (ACTAVIS ELIZABETH) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: OXYCODONE AND ACETAMINOPHEN; Active ingredients: ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE; Application number: ANDA04080
| Brand name | OXYCODONE AND ACETAMINOPHEN |
|---|---|
| Active ingredients | ACETAMINOPHEN; OXYCODONE HYDROCHLORIDE |
| Application number | ANDA040800 |
| Sponsor | ACTAVIS ELIZABETH |
| Dosage form | TABLET |
| Route | ORAL |
| Marketing status | Discontinued |
| Products in application | 2 |
| First approval date | 20120403 |
| Source | openFDA Drugs@FDA |
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