NDC 47335-794-81
Venlafaxine Hydrochloride 225 mg/1
Venlafaxine Hydrochloride · TABLET, EXTENDED RELEASE
Venlafaxine Hydrochloride is a tablet, extended release containing venlafaxine hydrochloride at a strength of 225 mg/1. Manufactured by Sun Pharmaceutical Industries, Inc..
Key Facts
- Brand Name
- Venlafaxine Hydrochloride
- Generic Name
- Venlafaxine Hydrochloride
- NDC Code (Package)
47335-794-81- NDC Code (Product)
47335-794- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Strength
- 225 mg/1
- Dosage Form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Marketing Status
- Application #
- ANDA091272
- Marketing Start
- 02/15/2019
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.