United States · FDA National Drug Code directory

Duloxetine

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: 68071-3766_2b61d5b5-490b-5494-e063-6294a90a3fa1
Product NDC: 68071-3766
Form: CAPSULE, DELAYED RELEASE
Composition / generic term: Duloxetine
Labeler: NuCare Pharmaceuticals, Inc.
Marketing category: ANDA
Marketing start / end (source format): 20170316
Source listing expiry: 20261231

Source-listed ingredients

DULOXETINE HYDROCHLORIDE — 30 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68071-3766-9) · 68071-3766-9

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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