Venlafaxine 70771-1649-09

Package NDC

70771-1649-09

Manufacturer: Zydus Lifesciences Limited
Dosage Form: Tablet, Extended Release
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: September 1, 2022
Listing Expires: December 31, 2026
Application: ANDA215622

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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

70771-1649-09Selected

90 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1649-9)

Other packages for this product(2)

70771-1649-01

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1649-1)

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70771-1649-03

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1649-3)

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