Venlafaxine Hydrochloride 68084-0698-01

Package NDC

68084-0698-01

Manufacturer: American Health Packaging
Dosage Form: Capsule, Extended Release
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: February 6, 2014
Listing Expires: December 31, 2026
Application: ANDA200834

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Active Ingredients

Ingredient	Strength
Venlafaxine Hydrochloride	37.5 mg/1

Drug Class

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

Selected Package

68084-0698-01Selected

100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-698-01) / 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (68084-698-11)