Duloxetine 82009-0031

Generic: Duloxetine Hydrochloride

Product NDC

82009-0031

Manufacturer: Quallent Pharmaceuticals Health, Llc
Dosage Form: Capsule, Delayed Release Pellets
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: May 21, 2018
Listing Expires: December 31, 2026
Application: ANDA203088

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Active Ingredients

Ingredient	Strength
Duloxetine Hydrochloride	40 mg/1

Drug Class

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

Packaging Options(1)

82009-0031-90

90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (82009-031-90)

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