Venlafaxine Hydrochloride 00093-9149-01

Package NDC

00093-9149-01

Manufacturer: Teva Pharmaceuticals Usa, Inc.
Dosage Form: Tablet
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: August 4, 2006
Listing Expires: December 31, 2026
Application: ANDA076690

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Active Ingredients

Ingredient	Strength
Venlafaxine Hydrochloride	50 mg/1

Drug Class

Norepinephrine Uptake Inhibitors [MoA]Serotonin Uptake Inhibitors [MoA]Serotonin and Norepinephrine Reuptake Inhibitor [EPC]

Selected Package

00093-9149-01Selected

100 TABLET in 1 BOTTLE (0093-9149-01)