← FDA Drug Approvals (Drugs@FDA)
VENLAFAXINE HYDROCHLORIDE
ANDA · Abbreviated New Drug Application (Generic) · Sponsor: AJANTA PHARMA LTD · Approved 2023-04-12
Drug application
- FDA Application #
ANDA214691- Application type
- Abbreviated New Drug Application (Generic)
- Brand name
- VENLAFAXINE HYDROCHLORIDE
- Generic name
- VENLAFAXINE
- Active ingredients
- VENLAFAXINE HYDROCHLORIDE
- Dosage form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Marketing status
- Prescription
- Sponsor
- AJANTA PHARMA LTD
- Manufacturer
- Ajanta Pharma USA Inc.
- First approval
- 2023-04-12
Source
- Authoritative
- Drugs@FDA application overview
- Machine
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