Venlafaxine Hydrochloride 82009-0056-10

Package NDC

82009-0056-10

Product NDC: 82009-0056

Manufacturer: Quallent Pharmaceuticals Health Llc
Dosage Form: Capsule, Extended Release
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: November 21, 2022
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

82009-0056-10Selected

1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (82009-056-10)