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
- 68788-4035_e6e275c3-1e16-4a00-b7fd-608ae6cbd515
- Product NDC
- 68788-4035
- Form
- TABLET, FILM COATED
- Composition / generic term
- Tramadol Hydrochloride
- Labeler
- Preferred Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250929
- 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 (68788-4035-1) · 68788-4035-1
- 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4035-2) · 68788-4035-2
- 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4035-3) · 68788-4035-3
- 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4035-4) · 68788-4035-4
- 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4035-5) · 68788-4035-5
- 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4035-6) · 68788-4035-6
- 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4035-7) · 68788-4035-7
- 120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4035-8) · 68788-4035-8
- 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4035-9) · 68788-4035-9
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →