NDC 71335-1964 – Duloxetine

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

Human Prescription Drug

Product NDC71335-1964

Product details

Brand name
Duloxetine
Generic name
Duloxetine
Labeler
Bryant Ranch Prepack
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA206653
Marketed since
January 20, 2016
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
71335-1964-130 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1964-1)Feb 10, 2021
71335-1964-260 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1964-2)Feb 10, 2021
71335-1964-328 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1964-3)Feb 10, 2021
71335-1964-490 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1964-4)Feb 10, 2021

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