NDC 68071-3779 – Duloxetine

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

Human Prescription Drug

Product NDC68071-3779

Product details

Brand name
Duloxetine
Generic name
Duloxetine
Labeler
NuCare Pharmaceuticals,Inc.
Dosage form
Capsule, Delayed Release Pellets
Route
Oral
Marketing category
ANDA · ANDA090776
Marketed since
December 17, 2013
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 (1)

Package NDCDescriptionSince
68071-3779-330 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68071-3779-3)Feb 6, 2025

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