NDC 87063-704 – Duloxetine

Duloxetine Hydrochloride 40 mg/1 · Capsule, Delayed Release · Oral

Human Prescription Drug

Product NDC87063-704

Product details

Brand name
Duloxetine
Generic name
Duloxetine
Labeler
ASCLEMED USA INC.
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA208706
Marketed since
March 25, 2019
Listing expires
December 31, 2027
Pharmacologic class
Serotonin and Norepinephrine Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Duloxetine →

Package NDC codes (4)

Package NDCDescriptionSince
87063-704-12120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (87063-704-12)Jul 2, 2026
87063-704-3030 CAPSULE, DELAYED RELEASE in 1 BOTTLE (87063-704-30)Jul 2, 2026
87063-704-6060 CAPSULE, DELAYED RELEASE in 1 BOTTLE (87063-704-60)Jul 2, 2026
87063-704-9090 CAPSULE, DELAYED RELEASE in 1 BOTTLE (87063-704-90)Jul 2, 2026

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