Duloxetine 82009-0173-10

Package NDC

82009-0173-10

Product NDC: 82009-0173

Manufacturer: Quallent Pharmaceuticals Health Llc
Dosage Form: Capsule, Delayed Release
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: July 1, 2025
Listing Expires: December 31, 2026
Application: ANDA208706

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Active Ingredients

Ingredient	Strength
Duloxetine Hydrochloride	60 mg/1

Drug Class

Norepinephrine Uptake Inhibitors [MoA]Serotonin Uptake Inhibitors [MoA]Serotonin and Norepinephrine Reuptake Inhibitor [EPC]

Selected Package

82009-0173-10Selected

1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (82009-173-10)