Duloxetine Delayed-Release 51991-0748-33

Generic: Duloxetine Hydrochloride

Package NDC

51991-0748-33

Product NDC: 51991-0748

Manufacturer: Breckenridge Pharmaceutical, Inc.
Dosage Form: Capsule, Delayed Release Pellets
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: June 11, 2014
Listing Expires: December 31, 2026
Application: ANDA203088

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Active Ingredients

Ingredient	Strength
Duloxetine Hydrochloride	60 mg/1

Drug Class

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

Selected Package

51991-0748-33Selected

30 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-748-33)

Other packages for this product(2)

51991-0748-10

1000 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-748-10)

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51991-0748-90

90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-748-90)

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