Duloxetine 68180-0295-09

Package NDC

68180-0295-09

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	30 mg/1

Drug Class

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

Selected Package

68180-0295-09Selected

90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68180-295-09)

Other packages for this product(2)

68180-0295-03

1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68180-295-03)

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68180-0295-06

30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68180-295-06)

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