NDC 71335-2624 – Duloxetine

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

Human Prescription Drug

Product NDC71335-2624

Product details

Brand name
Duloxetine
Generic name
Duloxetine
Labeler
Bryant Ranch Prepack
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA090694
Marketed since
December 11, 2013
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 (4)

Package NDCDescriptionSince
71335-2624-130 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2624-1)Jun 2, 2025
71335-2624-260 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2624-2)Jun 2, 2025
71335-2624-328 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2624-3)Jun 2, 2025
71335-2624-490 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2624-4)Jun 2, 2025

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