United States · FDA National Drug Code directory
ConZip
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
- 68025-072_50c36ee9-b6f1-4f50-a276-cfbfa49ba588
- Product NDC
- 68025-072
- Form
- CAPSULE, EXTENDED RELEASE
- Composition / generic term
- tramadol hydrochloride
- Labeler
- Vertical Pharmaceuticals, LLC
- Marketing category
- NDA
- Marketing start / end (source format)
- 20110920
- Source listing expiry
- 20261231
Source-listed ingredients
- TRAMADOL HYDROCHLORIDE — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68025-072-30) · 68025-072-30
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 →