Duloxetine D/r 72189-0634

Product NDC

72189-0634

Manufacturer: Direct_rx
Dosage Form: Capsule, Delayed Release
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: July 25, 2025
Listing Expires: December 31, 2026
Application: ANDA090694

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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)

72189-0634-30

30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (72189-634-30)

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