NDC 42708-196 – Duloxetine

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

Human Prescription Drug

Product NDC42708-196

Product details

Brand name
Duloxetine
Generic name
Duloxetine
Labeler
QPharma, 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 (1)

Package NDCDescriptionSince
42708-196-30 sample30 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (42708-196-30)Apr 10, 2026

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