NDC 50090-6899 – Duloxetine

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

Human Prescription Drug

Product NDC50090-6899

Product details

Brand name
Duloxetine
Generic name
Duloxetine
Labeler
A-S Medication Solutions
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA208706
Marketed since
March 16, 2017
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
50090-6899-030 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-6899-0)Dec 11, 2023
50090-6899-190 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-6899-1)Dec 11, 2023

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