Duloxetine Hydrochloride 50771-0203-02

Package NDC

50771-0203-02

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	60 mg/1

Drug Class

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

Selected Package

50771-0203-02Selected

500 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (50771-203-02)

Other packages for this product(1)

50771-0203-01

30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (50771-203-01)

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