Venlafaxine Hydrochloride 68071-5020-09

Package NDC

68071-5020-09

Manufacturer: Nucare Pharmaceuticals,inc.
Dosage Form: Capsule, Extended Release
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: November 23, 2011
Listing Expires: December 31, 2026
Application: ANDA200834

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Active Ingredients

Ingredient	Strength
Venlafaxine Hydrochloride	150 mg/1

Drug Class

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

Selected Package

68071-5020-09Selected

90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68071-5020-9)