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
- 71335-2612_064d5c7d-57b8-4bee-bcc6-739a2b2ad1b3
- Product NDC
- 71335-2612
- Form
- TABLET
- Composition / generic term
- tramadol hydrochloride
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180301
- Source listing expiry
- 20271231
Source-listed ingredients
- TRAMADOL HYDROCHLORIDE — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 8 TABLET in 1 BOTTLE (71335-2612-1) · 71335-2612-1
- 84 TABLET in 1 BOTTLE (71335-2612-2) · 71335-2612-2
- 56 TABLET in 1 BOTTLE (71335-2612-3) · 71335-2612-3
- 10 TABLET in 1 BOTTLE (71335-2612-4) · 71335-2612-4
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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