NDC 71205-445 – Duloxetine

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

Human Prescription Drug

Product NDC71205-445

Product details

Brand name
Duloxetine
Generic name
Duloxetine
Labeler
Proficient Rx LP
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA203197
Marketed since
May 1, 2012
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
71205-445-3030 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-445-30)May 19, 2020
71205-445-6060 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-445-60)May 19, 2020
71205-445-9090 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-445-90)May 19, 2020

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