Duloxetine 00615-8494

Product NDC

00615-8494

Manufacturer: Ncs Healthcare Of Ky, Llc Dba Vangard Labs
Dosage Form: Capsule, Delayed Release
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: December 11, 2013
Listing Expires: December 31, 2026
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]

Packaging Options(1)

00615-8494-39

30 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (0615-8494-39)

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