NDC 70710-1698-0
Venlafaxine Hydrochloride 37.5 mg/1
Venlafaxine Hydrochloride · CAPSULE, EXTENDED RELEASE
Venlafaxine Hydrochloride is a capsule, extended release containing venlafaxine hydrochloride at a strength of 37.5 mg/1. Manufactured by Zydus Pharmaceuticals USA Inc..
Key Facts
- Brand Name
- Venlafaxine Hydrochloride
- Generic Name
- Venlafaxine Hydrochloride
- NDC Code (Package)
70710-1698-0- NDC Code (Product)
70710-1698- Manufacturer
- Zydus Pharmaceuticals USA Inc.
- Strength
- 37.5 mg/1
- Dosage Form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Marketing Status
- Application #
- ANDA090174
- Marketing Start
- 05/18/2023
Recall History
No Recall HistoryView Full Drug Page
Venlafaxine Hydrochloride — All PackagesNot medical advice. This information is for reference only. Always consult your doctor or pharmacist.