NDC 71335-2017 – Duloxetine

Duloxetine Hydrochloride 30 mg/1 · Capsule, Delayed Release · Oral

Human Prescription Drug

Product NDC71335-2017

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, 2026
Pharmacologic class
Serotonin and Norepinephrine Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Duloxetine →

Package NDC codes (8)

Package NDCDescriptionSince
71335-2017-130 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2017-1)Feb 10, 2022
71335-2017-260 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2017-2)Feb 10, 2022
71335-2017-328 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2017-3)Feb 10, 2022
71335-2017-46 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2017-4)Feb 10, 2022
71335-2017-590 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2017-5)Feb 10, 2022
71335-2017-615 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2017-6)Feb 10, 2022
71335-2017-7180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2017-7)Feb 10, 2022
71335-2017-8120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2017-8)Feb 10, 2022

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