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
- 68788-4040_f558c59c-cbd4-4b17-9a3d-b014ad09bbb1
- Product NDC
- 68788-4040
- Form
- TABLET, FILM COATED
- Composition / generic term
- Tramadol Hydrochloride
- Labeler
- Preferred Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20251013
- Source listing expiry
- 20261231
Source-listed ingredients
- TRAMADOL HYDROCHLORIDE — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4040-1) · 68788-4040-1
- 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4040-2) · 68788-4040-2
- 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4040-3) · 68788-4040-3
- 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4040-4) · 68788-4040-4
- 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4040-5) · 68788-4040-5
- 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4040-6) · 68788-4040-6
- 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4040-7) · 68788-4040-7
- 120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4040-8) · 68788-4040-8
- 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4040-9) · 68788-4040-9
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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