Duloxetine Delayed-Release 70518-0122

Generic: Duloxetine Hydrochloride

Product NDC

70518-0122

Manufacturer: Remedyrepack Inc.
Dosage Form: Capsule, Delayed Release Pellets
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: January 13, 2017
Listing Expires: December 31, 2027
Application: ANDA203088

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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]

Packaging Options(1)

70518-0122-05

90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (70518-0122-5)

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