NDC 68788-4128 – Duloxetine

Duloxetine Hydrochloride 20 mg/1 · Capsule, Delayed Release · Oral

Human Prescription Drug

Product NDC68788-4128

Product details

Brand name
Duloxetine
Generic name
Duloxetine
Labeler
Preferred Pharmaceuticals Inc.
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA208706
Marketed since
June 10, 2026
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 (3)

Package NDCDescriptionSince
68788-4128-330 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-4128-3)Jun 10, 2026
68788-4128-660 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-4128-6)Jun 10, 2026
68788-4128-990 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-4128-9)Jun 10, 2026

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