Venlafaxine Hydrochloride 69367-0417-30

Package NDC

69367-0417-30

Manufacturer: Westminster Pharmaceuticals, Llc
Dosage Form: Tablet, Extended Release
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: November 18, 2025
Listing Expires: December 31, 2026
Application: ANDA205468

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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

69367-0417-30Selected

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (69367-417-30)

Other packages for this product(1)

69367-0417-09

90 TABLET, EXTENDED RELEASE in 1 BOTTLE (69367-417-09)

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