NAFTIFINE HYDROCHLORIDE (NAFTIFINE HYDROCHLORIDE) — FDA Approval ANDA208201 (SUN PHARMA CANADA)
NAFTIFINE HYDROCHLORIDE (NAFTIFINE HYDROCHLORIDE) — FDA Approval ANDA208201 (SUN PHARMA CANADA) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: NAFTIFINE HYDROCHLORIDE; Active ingredients: NAFTIFINE HYDROCHLORIDE; Application number: ANDA208201.
| Brand name | NAFTIFINE HYDROCHLORIDE |
|---|---|
| Active ingredients | NAFTIFINE HYDROCHLORIDE |
| Application number | ANDA208201 |
| Sponsor | SUN PHARMA CANADA |
| Dosage form | GEL |
| Route | TOPICAL |
| Marketing status | Prescription |
| Products in application | 1 |
| First approval date | 20190410 |
| Source | openFDA Drugs@FDA |
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