Duloxetine 71610-0401

Generic: Duloxetine Hydrochloride

Product NDC

71610-0401

Manufacturer: Aphena Pharma Solutions - Tennessee, Llc
Dosage Form: Capsule, Delayed Release
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: December 11, 2013
Listing Expires: December 31, 2026
Application: ANDA090778

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Active Ingredients

Ingredient	Strength
Duloxetine Hydrochloride	20 mg/1

Drug Class

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

Packaging Options(1)

71610-0401-83

3600 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71610-401-83)

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