Drugplain

NDC 70710-1700-0

Venlafaxine Hydrochloride 150 mg/1

Venlafaxine Hydrochloride · CAPSULE, EXTENDED RELEASE

No Recall History

Venlafaxine Hydrochloride is a capsule, extended release containing venlafaxine hydrochloride at a strength of 150 mg/1. Manufactured by Zydus Pharmaceuticals USA Inc..

Key Facts

Brand Name
Venlafaxine Hydrochloride
Generic Name
Venlafaxine Hydrochloride
NDC Code (Package)
70710-1700-0
NDC Code (Product)
70710-1700
Manufacturer
Zydus Pharmaceuticals USA Inc.
Strength
150 mg/1
Dosage Form
CAPSULE, EXTENDED RELEASE
Route
ORAL
Marketing Status
Application #
ANDA090174
Marketing Start
05/18/2023

Recall History

No Recall History

Not medical advice. This information is for reference only. Always consult your doctor or pharmacist.