NDC 80425-0389 – Duloxetine

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

Human Prescription Drug

Product NDC80425-0389

Product details

Brand name
Duloxetine
Generic name
Duloxetine
Labeler
Advanced Rx of Tennessee, LLC
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA090694
Marketed since
May 22, 2024
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
80425-0389-130 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0389-1)May 22, 2024
80425-0389-260 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0389-2)May 22, 2024
80425-0389-390 CAPSULE, DELAYED RELEASE in 1 BOTTLE (80425-0389-3)May 22, 2024

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