Duloxetine Hydrochloride 50771-0201-01

Package NDC

50771-0201-01

Manufacturer: Yaopharma Co., Ltd.
Dosage Form: Capsule, Delayed Release Pellets
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: January 1, 2024
Listing Expires: December 31, 2026
Application: ANDA207219

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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]

Selected Package

50771-0201-01Selected

60 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (50771-201-01)