Duloxetine 68180-0294-03

Package NDC

68180-0294-03

Manufacturer: Lupin Pharmaceuticals, Inc.
Dosage Form: Capsule, Delayed Release
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: December 11, 2013
Listing Expires: December 31, 2027
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]

Selected Package

68180-0294-03Selected

1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68180-294-03)

Other packages for this product(1)

68180-0294-07

60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68180-294-07)

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