Duloxetine Hydrochloride 33342-0161-44

Package NDC

33342-0161-44

Manufacturer: Macleods Pharmaceuticals Limited
Dosage Form: Capsule, Delayed Release
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: March 24, 2017
Listing Expires: December 31, 2026
Application: ANDA204815

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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

33342-0161-44Selected

1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (33342-161-44)

Other packages for this product(3)

33342-0161-07

30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (33342-161-07)

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33342-0161-10

90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (33342-161-10)

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33342-0161-12

10 BLISTER PACK in 1 CARTON (33342-161-12) / 10 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK

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