NDC 43547-381 – Duloxetine

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

Human Prescription Drug

Product NDC43547-381

Product details

Brand name
Duloxetine
Generic name
Duloxetine
Labeler
Solco Healthcare US, LLC
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA206653
Marketed since
January 20, 2016
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
43547-381-0330 CAPSULE, DELAYED RELEASE in 1 BOTTLE (43547-381-03)Jan 20, 2016
43547-381-0990 CAPSULE, DELAYED RELEASE in 1 BOTTLE (43547-381-09)Jan 20, 2016
43547-381-111000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (43547-381-11)Jan 20, 2016

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