NDC 68788-8623 – Duloxetine

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

Human Prescription Drug

Product NDC68788-8623

Product details

Brand name
Duloxetine
Generic name
Duloxetine
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA090694
Marketed since
April 8, 2024
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
68788-8623-330 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8623-3)Apr 8, 2024
68788-8623-660 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8623-6)Apr 8, 2024
68788-8623-990 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-8623-9)Apr 8, 2024

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