NDC 71205-358 – Duloxetine

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

Human Prescription Drug

Product NDC71205-358

Product details

Brand name
Duloxetine
Generic name
Duloxetine
Labeler
Proficient Rx LP
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 (3)

Package NDCDescriptionSince
71205-358-3030 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-358-30)Nov 14, 2019
71205-358-6060 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-358-60)Nov 14, 2019
71205-358-9090 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-358-90)Nov 14, 2019

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