NDC 71335-3062 – Duloxetine

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

Human Prescription Drug

Product NDC71335-3062

Product details

Brand name
Duloxetine
Generic name
Duloxetine
Labeler
Bryant Ranch Prepack
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA208706
Marketed since
March 16, 2017
Listing expires
December 31, 2027
Pharmacologic class
Serotonin and Norepinephrine Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Duloxetine →

Package NDC codes (4)

Package NDCDescriptionSince
71335-3062-130 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-3062-1)Feb 6, 2026
71335-3062-260 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-3062-2)Feb 6, 2026
71335-3062-328 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-3062-3)Feb 6, 2026
71335-3062-490 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-3062-4)Feb 6, 2026

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