NDC 50090-6889 – Duloxetine Delayed-Release

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

Human Prescription Drug

Product NDC50090-6889

Product details

Brand name
Duloxetine Delayed-Release
Generic name
Duloxetine Hydrochloride
Labeler
A-S Medication Solutions
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 (2)

Package NDCDescriptionSince
50090-6889-090 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (50090-6889-0)Dec 6, 2023
50090-6889-130 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (50090-6889-1)Dec 6, 2023

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