NDC 51407-810 – Duloxetine

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

Human Prescription Drug

Product NDC51407-810

Product details

Brand name
Duloxetine
Generic name
Duloxetine
Labeler
Golden State Medical Supply, Inc.
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA090694
Marketed since
December 11, 2013
Listing expires
December 31, 2027
Pharmacologic class
Serotonin and Norepinephrine Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Duloxetine →

Package NDC codes (3)

Package NDCDescriptionSince
51407-810-101000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (51407-810-10)Jul 10, 2026
51407-810-3030 CAPSULE, DELAYED RELEASE in 1 BOTTLE (51407-810-30)Jul 10, 2026
51407-810-9090 CAPSULE, DELAYED RELEASE in 1 BOTTLE (51407-810-90)Jul 10, 2026

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