NDC 71610-739 – Duloxetine Delayed-Release

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

Human Prescription Drug

Product NDC71610-739

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 (3)

Package NDCDescriptionSince
71610-739-166000 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71610-739-16)Jan 8, 2024
71610-739-33840 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71610-739-33)Mar 22, 2024
71610-739-74500 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (71610-739-74)Sep 27, 2023

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