Venlafaxine Hydrochloride 68382-0036-06

Package NDC

68382-0036-06

Manufacturer: Zydus Pharmaceuticals Usa Inc.
Dosage Form: Capsule, Extended Release
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: June 1, 2011
Listing Expires: December 31, 2026
Application: ANDA090174

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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

68382-0036-06Selected

30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68382-036-06)

Other packages for this product(2)

68382-0036-10

1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68382-036-10)

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68382-0036-16

90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68382-036-16)

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