Venlafaxine Hydrochloride 65841-0753-16

Package NDC

65841-0753-16

Manufacturer: Zydus Lifesciences Limited
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

65841-0753-16Selected

90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65841-753-16)

Other packages for this product(2)

65841-0753-06

30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65841-753-06)

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65841-0753-10

1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65841-753-10)

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