NDC 68071-3766 – Duloxetine

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

Human Prescription Drug

Product NDC68071-3766

Product details

Brand name
Duloxetine
Generic name
Duloxetine
Labeler
NuCare Pharmaceuticals, Inc.
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA208706
Marketed since
March 16, 2017
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
68071-3766-990 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-3766-9)Jan 10, 2025

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