NDC 82804-024 – Duloxetine Delayed-Release

Duloxetine Hydrochloride 40 mg/1 · Capsule, Delayed Release Pellets · Oral

Human Prescription Drug

Product NDC82804-024

Product details

Brand name
Duloxetine Delayed-Release
Generic name
Duloxetine Hydrochloride
Labeler
Proficient Rx LP
Dosage form
Capsule, Delayed Release Pellets
Route
Oral
Marketing category
ANDA · ANDA203088
Marketed since
May 21, 2018
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
82804-024-3030 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (82804-024-30)Oct 16, 2023
82804-024-6060 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (82804-024-60)Oct 16, 2023
82804-024-9090 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (82804-024-90)Oct 16, 2023

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