DONEPEZIL HYDROCHLORIDE (DONEPEZIL HYDROCHLORIDE) — FDA Approval ANDA077975 (SUN PHARM INDUSTRIES)
DONEPEZIL HYDROCHLORIDE (DONEPEZIL HYDROCHLORIDE) — FDA Approval ANDA077975 (SUN PHARM INDUSTRIES) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: DONEPEZIL HYDROCHLORIDE; Active ingredients: DONEPEZIL HYDROCHLORIDE; Application number: ANDA077975.
| Brand name | DONEPEZIL HYDROCHLORIDE |
|---|---|
| Active ingredients | DONEPEZIL HYDROCHLORIDE |
| Application number | ANDA077975 |
| Sponsor | SUN PHARM INDUSTRIES |
| Dosage form | TABLET, ORALLY DISINTEGRATING |
| Route | ORAL |
| Marketing status | Discontinued |
| Products in application | 2 |
| First approval date | 20091211 |
| Source | openFDA Drugs@FDA |
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