Drugplain

NDC 68084-709-01

Venlafaxine Hydrochloride 75 mg/1

Venlafaxine Hydrochloride · CAPSULE, EXTENDED RELEASE

No Recall History

Venlafaxine Hydrochloride is a capsule, extended release containing venlafaxine hydrochloride at a strength of 75 mg/1. Manufactured by American Health Packaging.

Key Facts

Brand Name
Venlafaxine Hydrochloride
Generic Name
Venlafaxine Hydrochloride
NDC Code (Package)
68084-709-01
NDC Code (Product)
68084-709
Manufacturer
American Health Packaging
Strength
75 mg/1
Dosage Form
CAPSULE, EXTENDED RELEASE
Route
ORAL
Marketing Status
Application #
ANDA200834
Marketing Start
06/03/2014

Recall History

No Recall History

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