NDC 70954-861 – Duloxetine

Duloxetine Hydrochloride 30 mg/1 · Capsule, Delayed Release · Oral

Human Prescription Drug

Product NDC70954-861

Product details

Brand name
Duloxetine
Generic name
Duloxetine
Labeler
ANI Pharmaceuticals, Inc.
Dosage form
Capsule, Delayed Release
Route
Oral
Marketing category
ANDA · ANDA202336
Marketed since
July 13, 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 (1)

Package NDCDescriptionSince
70954-861-2090 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70954-861-20)Jul 13, 2026

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