NALTREXONE HYDROCHLORIDE (NALTREXONE HYDROCHLORIDE) — FDA Approval ANDA075434 (NOVITIUM PHARMA)
NALTREXONE HYDROCHLORIDE (NALTREXONE HYDROCHLORIDE) — FDA Approval ANDA075434 (NOVITIUM PHARMA) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: NALTREXONE HYDROCHLORIDE; Active ingredients: NALTREXONE HYDROCHLORIDE; Application number: ANDA075434.
| Brand name | NALTREXONE HYDROCHLORIDE |
|---|---|
| Active ingredients | NALTREXONE HYDROCHLORIDE |
| Application number | ANDA075434 |
| Sponsor | NOVITIUM PHARMA |
| Dosage form | TABLET |
| Route | ORAL |
| Marketing status | Discontinued |
| Products in application | 1 |
| First approval date | 20000308 |
| Source | openFDA Drugs@FDA |
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