United States · FDA National Drug Code directory

Tramadol Hydrochloride

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: 68180-383_e674f8e1-d70a-4e39-b2c3-6b7ad77e3796
Product NDC: 68180-383
Form: TABLET, EXTENDED RELEASE
Composition / generic term: Tramadol Hydrochloride
Labeler: Lupin Pharmaceuticals, Inc.
Marketing category: ANDA
Marketing start / end (source format): 20110926
Source listing expiry: 20261231

Source-listed ingredients

TRAMADOL HYDROCHLORIDE — 100 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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