Duloxetine 42708-0196-30

Package NDC

42708-0196-30

Manufacturer: Qpharma, Inc.
Dosage Form: Capsule, Delayed Release
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: December 11, 2013
Listing Expires: December 31, 2027
Application: ANDA090694

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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

42708-0196-30Selected

30 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (42708-196-30)