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
- 71335-2518_e37a5865-f78e-41d4-9d0a-b7ec7bcd0807
- Product NDC
- 71335-2518
- Form
- TABLET
- Composition / generic term
- tramadol hydrochloride
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20180301
- Source listing expiry
- 20261231
Source-listed ingredients
- TRAMADOL HYDROCHLORIDE — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 50 TABLET in 1 BOTTLE (71335-2518-0) · 71335-2518-0
- 30 TABLET in 1 BOTTLE (71335-2518-1) · 71335-2518-1
- 20 TABLET in 1 BOTTLE (71335-2518-2) · 71335-2518-2
- 90 TABLET in 1 BOTTLE (71335-2518-3) · 71335-2518-3
- 60 TABLET in 1 BOTTLE (71335-2518-4) · 71335-2518-4
- 120 TABLET in 1 BOTTLE (71335-2518-5) · 71335-2518-5
- 180 TABLET in 1 BOTTLE (71335-2518-6) · 71335-2518-6
- 40 TABLET in 1 BOTTLE (71335-2518-7) · 71335-2518-7
- 100 TABLET in 1 BOTTLE (71335-2518-8) · 71335-2518-8
- 15 TABLET in 1 BOTTLE (71335-2518-9) · 71335-2518-9
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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