NDC 71335-1672 – Duloxetine

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

Human Prescription Drug

Product NDC71335-1672

Product details

Brand name
Duloxetine
Generic name
Duloxetine
Labeler
Bryant Ranch Prepack
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA203197
Marketed since
May 1, 2012
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
71335-1672-130 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1672-1)Jul 27, 2020
71335-1672-260 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1672-2)Aug 28, 2020
71335-1672-328 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1672-3)Apr 4, 2024
71335-1672-46 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1672-4)Apr 4, 2024
71335-1672-590 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1672-5)Dec 22, 2020
71335-1672-615 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1672-6)Jan 7, 2021
71335-1672-7180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1672-7)Feb 1, 2021
71335-1672-8120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1672-8)Apr 4, 2024

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