NDC 85534-0051 – Duloxetine

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

Human Prescription Drug

Product NDC85534-0051

Product details

Brand name
Duloxetine
Generic name
Duloxetine
Labeler
HAWAII REPACK, INC
Dosage form
Capsule, Delayed Release Pellets
Route
Oral
Marketing category
ANDA · ANDA090776
Marketed since
December 17, 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 (4)

Package NDCDescriptionSince
85534-0051-030 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (85534-0051-0)Jul 2, 2026
85534-0051-160 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (85534-0051-1)Jul 2, 2026
85534-0051-290 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (85534-0051-2)Jul 2, 2026
85534-0051-3120 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (85534-0051-3)Jul 2, 2026

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