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
- 60760-727_55a68838-257b-fdea-e063-6394a90ac8e0
- Product NDC
- 60760-727
- Form
- TABLET
- Composition / generic term
- Tramadol Hydrochloride
- Labeler
- St. Mary's Medical Park Pharmacy
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20251105
- Source listing expiry
- 20271231
Source-listed ingredients
- TRAMADOL HYDROCHLORIDE — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 9 TABLET in 1 BOTTLE, PLASTIC (60760-727-09) · 60760-727-09
- 20 TABLET in 1 BOTTLE, PLASTIC (60760-727-20) · 60760-727-20
- 30 TABLET in 1 BOTTLE, PLASTIC (60760-727-30) · 60760-727-30
- 50 TABLET in 1 BOTTLE, PLASTIC (60760-727-50) · 60760-727-50
- 60 TABLET in 1 BOTTLE, PLASTIC (60760-727-60) · 60760-727-60
- 90 TABLET in 1 BOTTLE, PLASTIC (60760-727-90) · 60760-727-90
- 120 TABLET in 1 BOTTLE, PLASTIC (60760-727-92) · 60760-727-92
- 180 TABLET in 1 BOTTLE, PLASTIC (60760-727-98) · 60760-727-98
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 →