Duloxetine 70247-0012-06

Package NDC

70247-0012-06

Manufacturer: Qingdao Baheal Pharmaceutical Co., Ltd.
Dosage Form: Capsule, Delayed Release
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: May 5, 2018
Listing Expires: December 31, 2026
Application: ANDA210599

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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

70247-0012-06Selected

60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70247-012-06)