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
- 63629-8323_1bb0af50-74d6-49a3-b954-760eadfe4bf2
- Product NDC
- 63629-8323
- Form
- TABLET, EXTENDED RELEASE
- Composition / generic term
- TRAMADOL HYDROCHLORIDE
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20140819
- Source listing expiry
- 20261231
Source-listed ingredients
- TRAMADOL HYDROCHLORIDE — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-8323-1) · 63629-8323-1
- 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-8323-2) · 63629-8323-2
- 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-8323-3) · 63629-8323-3
- 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-8323-4) · 63629-8323-4
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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