Duloxetine 65841-0799-14

Package NDC

65841-0799-14

Manufacturer: Zydus Lifesciences Limited
Dosage Form: Capsule, Delayed Release
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: May 27, 2014
Listing Expires: December 31, 2026
Application: ANDA090739

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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

65841-0799-14Selected

60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-799-14)

Other packages for this product(2)

65841-0799-06

30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-799-06)

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65841-0799-16

90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (65841-799-16)

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