NDC 71335-2537 – Duloxetine

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

Human Prescription Drug

Product NDC71335-2537

Product details

Brand name
Duloxetine
Generic name
Duloxetine
Labeler
Bryant Ranch Prepack
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA090694
Marketed since
December 11, 2013
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
71335-2537-130 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2537-1)Dec 10, 2024
71335-2537-260 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2537-2)Dec 10, 2024
71335-2537-328 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2537-3)Dec 10, 2024
71335-2537-46 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2537-4)Dec 10, 2024
71335-2537-590 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2537-5)Dec 10, 2024
71335-2537-615 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2537-6)Dec 10, 2024
71335-2537-7180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2537-7)Dec 10, 2024
71335-2537-8120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-2537-8)Dec 10, 2024

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