NDC 72789-338 – Duloxetine

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

Human Prescription Drug

Product NDC72789-338

Product details

Brand name
Duloxetine
Generic name
Duloxetine
Labeler
PD-Rx Pharmaceuticals, Inc.
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA208706
Marketed since
March 16, 2017
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 (1)

Package NDCDescriptionSince
72789-338-9090 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72789-338-90)Jul 28, 2023

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