NDC 63187-612 – Duloxetine

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

Human Prescription Drug

Product NDC63187-612

Product details

Brand name
Duloxetine
Generic name
Duloxetine Hydrochloride
Labeler
Proficient Rx LP
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA090778
Marketed since
December 11, 2013
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
63187-612-3030 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-612-30)Dec 1, 2018
63187-612-6060 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-612-60)Dec 1, 2018
63187-612-9090 CAPSULE, DELAYED RELEASE in 1 BOTTLE (63187-612-90)Dec 1, 2018

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