VENLAFAXINE HYDROCHLORIDE (VENLAFAXINE HYDROCHLORIDE) — FDA Approval ANDA090174 (ZYDUS PHARMS USA INC)
VENLAFAXINE HYDROCHLORIDE (VENLAFAXINE HYDROCHLORIDE) — FDA Approval ANDA090174 (ZYDUS PHARMS USA INC) is one of 9,000 drug approvals in the DrugApprovals dataset. Key details — Brand name: VENLAFAXINE HYDROCHLORIDE; Active ingredients: VENLAFAXINE HYDROCHLORIDE; Application number: ANDA090174.
| Brand name | VENLAFAXINE HYDROCHLORIDE |
|---|---|
| Active ingredients | VENLAFAXINE HYDROCHLORIDE |
| Application number | ANDA090174 |
| Sponsor | ZYDUS PHARMS USA INC |
| Dosage form | CAPSULE, EXTENDED RELEASE |
| Route | ORAL |
| Marketing status | Prescription |
| Products in application | 3 |
| First approval date | 20110414 |
| Source | openFDA Drugs@FDA |
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