NDC 85534-0016 – Duloxetine

Duloxetine Hydrochloride 20 mg/1 · Capsule, Delayed Release · Oral

Human Prescription Drug

Product NDC85534-0016

Product details

Brand name
Duloxetine
Generic name
Duloxetine
Labeler
HAWAII REPACK, INC.
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA208706
Marketed since
March 16, 2017
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 (4)

Package NDCDescriptionSince
85534-0016-030 CAPSULE, DELAYED RELEASE in 1 BOTTLE (85534-0016-0)Jul 2, 2026
85534-0016-160 CAPSULE, DELAYED RELEASE in 1 BOTTLE (85534-0016-1)Jul 2, 2026
85534-0016-290 CAPSULE, DELAYED RELEASE in 1 BOTTLE (85534-0016-2)Jul 2, 2026
85534-0016-3120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (85534-0016-3)Jul 2, 2026

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