MOTOFEN HALF-STRENGTH (ATROPINE SULFATE; DIFENOXIN HYDROCHLORID) — FDA Approval NDA017744 (LEGACY PHARMA)
MOTOFEN HALF-STRENGTH (ATROPINE SULFATE; DIFENOXIN HYDROCHLORID) — FDA Approval NDA017744 (LEGACY PHARMA) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: MOTOFEN HALF-STRENGTH; Active ingredients: ATROPINE SULFATE; DIFENOXIN HYDROCHLORIDE; Application number: NDA017744.
| Brand name | MOTOFEN HALF-STRENGTH |
|---|---|
| Active ingredients | ATROPINE SULFATE; DIFENOXIN HYDROCHLORIDE |
| Application number | NDA017744 |
| Sponsor | LEGACY PHARMA |
| Dosage form | TABLET |
| Route | ORAL |
| Marketing status | Discontinued |
| Products in application | 2 |
| First approval date | 19780714 |
| Source | openFDA Drugs@FDA |
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