NDC 62332-279 – Duloxetine Hydrochloride

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

Human Prescription Drug

Product NDC62332-279

Product details

Brand name
Duloxetine Hydrochloride
Generic name
Duloxetine
Labeler
Alembic Pharmaceuticals Inc.
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA202949
Marketed since
April 9, 2026
Listing expires
December 31, 2027
Pharmacologic class
Serotonin and Norepinephrine Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Duloxetine Hydrochloride →

Package NDC codes (3)

Package NDCDescriptionSince
62332-279-3030 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62332-279-30)Apr 9, 2026
62332-279-9090 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62332-279-90)Apr 9, 2026
62332-279-911000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (62332-279-91)Apr 9, 2026

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