United States · FDA National Drug Code directory
Trazodone 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
- 69584-885_79ac55b1-207c-4d5b-8fe4-9c91e99ca0a6
- Product NDC
- 69584-885
- Form
- TABLET, FILM COATED
- Composition / generic term
- Trazodone Hydrochloride
- Labeler
- Oxford Pharmaceuticals, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20230301
- Source listing expiry
- 20271231
Source-listed ingredients
- TRAZODONE HYDROCHLORIDE — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69584-885-09) · 69584-885-09
- 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69584-885-10) · 69584-885-10
- 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69584-885-50) · 69584-885-50
- 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69584-885-90) · 69584-885-90
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 →