NDC 46708-278 – Duloxetine Hydrochloride

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

Human Prescription Drug

Product NDC46708-278

Product details

Brand name
Duloxetine Hydrochloride
Generic name
Duloxetine
Labeler
Alembic Pharmaceuticals Limited
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA202949
Marketed since
June 9, 2014
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 (4)

Package NDCDescriptionSince
46708-278-3030 CAPSULE, DELAYED RELEASE in 1 BOTTLE (46708-278-30)Jun 9, 2014
46708-278-6060 CAPSULE, DELAYED RELEASE in 1 BOTTLE (46708-278-60)Jun 9, 2014
46708-278-9090 CAPSULE, DELAYED RELEASE in 1 BOTTLE (46708-278-90)Jun 9, 2014
46708-278-911000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (46708-278-91)Apr 9, 2026

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