NDC 68788-8362 – Duloxetine Delayed-Release

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

Human Prescription Drug

Product NDC68788-8362

Product details

Brand name
Duloxetine Delayed-Release
Generic name
Duloxetine Hydrochloride
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Capsule, Delayed Release Pellets
Route
Oral
Marketing category
ANDA · ANDA203088
Marketed since
February 1, 2023
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
68788-8362-060 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68788-8362-0)Mar 14, 2023
68788-8362-330 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68788-8362-3)Feb 1, 2023
68788-8362-990 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (68788-8362-9)Feb 1, 2023

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