United States · FDA National Drug Code directory

Cymbalta

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference: 0002-3240_aa5061b1-f237-425a-9d05-575c333dfd37
Product NDC: 0002-3240
Form: CAPSULE, DELAYED RELEASE
Composition / generic term: Duloxetine hydrochloride
Labeler: Eli Lilly and Company
Marketing category: NDA
Marketing start / end (source format): 20040824 / 20261002

Source-listed ingredients

DULOXETINE HYDROCHLORIDE — 30 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

Package details are not available in this snapshot.

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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