NDC 75834-219-30
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 Nivagen Pharmaceuticals, Inc..
Key Facts
- Brand Name
- VENLAFAXINE HYDROCHLORIDE
- Generic Name
- VENLAFAXINE HYDROCHLORIDE
- NDC Code (Package)
75834-219-30- NDC Code (Product)
75834-219- Manufacturer
- Nivagen Pharmaceuticals, Inc.
- Strength
- 225 mg/1
- Dosage Form
- TABLET, EXTENDED RELEASE
- Route
- ORAL
- Marketing Status
- Application #
- ANDA211323
- Marketing Start
- 09/06/2019
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.