United States · FDA National Drug Code directory

TRAMADOL HCL ER

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: 61919-818_24ac4469-6ec1-7d80-e063-6394a90aacf5
Product NDC: 61919-818
Form: TABLET, EXTENDED RELEASE
Composition / generic term: TRAMADOL HCL
Labeler: DIRECT RX
Marketing category: ANDA
Marketing start / end (source format): 20190503
Source listing expiry: 20261231

Source-listed ingredients

TRAMADOL HYDROCHLORIDE — 100 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (61919-818-30) · 61919-818-30
60 TABLET, EXTENDED RELEASE in 1 BOTTLE (61919-818-60) · 61919-818-60
90 TABLET, EXTENDED RELEASE in 1 BOTTLE (61919-818-90) · 61919-818-90

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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