NDC 71610-743 – Duloxetine Delayed-Release

Duloxetine Hydrochloride 60 mg/1 · Capsule, Delayed Release Pellets · Oral

Human Prescription Drug

Product NDC71610-743

Product details

Brand name
Duloxetine Delayed-Release
Generic name
Duloxetine Hydrochloride
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Dosage form
Capsule, Delayed Release Pellets
Route
Oral
Marketing category
ANDA · ANDA203088
Marketed since
June 11, 2014
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 (5)

Package NDCDescriptionSince
71610-743-3030 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71610-743-30)Oct 16, 2023
71610-743-5360 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71610-743-53)Oct 16, 2023
71610-743-6090 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71610-743-60)Oct 16, 2023
71610-743-74500 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71610-743-74)Jun 5, 2025
71610-743-80180 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71610-743-80)Mar 20, 2024

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