NDC 51407-819 – Duloxetine Delayed-Release

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

Human Prescription Drug

Product NDC51407-819

Product details

Brand name
Duloxetine Delayed-Release
Generic name
Duloxetine Hydrochloride
Labeler
Golden State Medical Supply, Inc.
Dosage form
Capsule, Delayed Release Pellets
Route
Oral
Marketing category
ANDA · ANDA203088
Marketed since
June 11, 2014
Marketing end
November 30, 2027
Pharmacologic class
Serotonin and Norepinephrine Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Duloxetine →

Package NDC codes (2)

Package NDCDescriptionSince
51407-819-101000 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51407-819-10)Jul 12, 2023
51407-819-3030 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51407-819-30)Jul 12, 2023

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