NDC 60760-759 – Duloxetine

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

Human Prescription Drug

Product NDC60760-759

Product details

Brand name
Duloxetine
Generic name
Duloxetine
Labeler
St. Mary's Medical Park Pharmacy
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA208706
Marketed since
July 15, 2025
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
60760-759-3030 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-759-30)Jul 15, 2025

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