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
- 47335-860_a994e116-d201-47f9-baaf-dd76a84eba7e
- Product NDC
- 47335-860
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- TRAMADOL HYDROCHLORIDE
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20111212
- Source listing expiry
- 20261231
Source-listed ingredients
- TRAMADOL HYDROCHLORIDE — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-860-08) · 47335-860-08
- 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-860-18) · 47335-860-18
- 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-860-83) · 47335-860-83
- 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-860-88) · 47335-860-88
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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