IMIPRAMINE HYDROCHLORIDE (IMIPRAMINE HYDROCHLORIDE) — FDA Approval ANDA081050 (SUN PHARM INDUSTRIES)
IMIPRAMINE HYDROCHLORIDE (IMIPRAMINE HYDROCHLORIDE) — FDA Approval ANDA081050 (SUN PHARM INDUSTRIES) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: IMIPRAMINE HYDROCHLORIDE; Active ingredients: IMIPRAMINE HYDROCHLORIDE; Application number: ANDA081050.
| Brand name | IMIPRAMINE HYDROCHLORIDE |
|---|---|
| Active ingredients | IMIPRAMINE HYDROCHLORIDE |
| Application number | ANDA081050 |
| Sponsor | SUN PHARM INDUSTRIES |
| Dosage form | TABLET |
| Route | ORAL |
| Marketing status | Prescription |
| Products in application | 1 |
| First approval date | 19900605 |
| Source | openFDA Drugs@FDA |
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