ORPHENADRINE CITRATE (ORPHENADRINE CITRATE) — FDA Approval ANDA087062 (WATSON LABS)
ORPHENADRINE CITRATE (ORPHENADRINE CITRATE) — FDA Approval ANDA087062 (WATSON LABS) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: ORPHENADRINE CITRATE; Active ingredients: ORPHENADRINE CITRATE; Application number: ANDA087062.
| Brand name | ORPHENADRINE CITRATE |
|---|---|
| Active ingredients | ORPHENADRINE CITRATE |
| Application number | ANDA087062 |
| Sponsor | WATSON LABS |
| Dosage form | INJECTABLE |
| Route | INJECTION |
| Marketing status | Discontinued |
| Products in application | 1 |
| First approval date | 19810716 |
| Source | openFDA Drugs@FDA |
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