NDC 80425-0311 – Duloxetine DR

Duloxetine Hydrochloride 20 mg/1 · Capsule, Delayed Release · Oral

Human Prescription Drug

Product NDC80425-0311

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
April 7, 2023
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
80425-0311-130 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0311-1)Apr 7, 2023
80425-0311-260 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0311-2)Apr 7, 2023
80425-0311-390 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0311-3)Apr 7, 2023

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