NDC 80425-0119 – Duloxetine DR

Duloxetine Hydrochloride 60 mg/1 · Capsule, Delayed Release · Oral

Human Prescription Drug

Product NDC80425-0119

Product details

Brand name
Duloxetine DR
Generic name
Duloxetine
Labeler
Advanced Rx Pharmacy of Tennessee, LLC
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA208706
Marketed since
March 16, 2017
Listing expires
December 31, 2026
Pharmacologic class
Serotonin and Norepinephrine Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Duloxetine →

Package NDC codes (3)

Package NDCDescriptionSince
80425-0119-130 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0119-1)Mar 16, 2017
80425-0119-260 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0119-2)Mar 16, 2017
80425-0119-330 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0119-3)Mar 30, 2023

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