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
- 71335-0742_337bd3ea-ccd3-7ae8-e063-6394a90a9b8f
- Product NDC
- 71335-0742
- Form
- TABLET
- Composition / generic term
- Trazodone Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20171211
- Source listing expiry
- 20261231
Source-listed ingredients
- TRAZODONE HYDROCHLORIDE — 150 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE (71335-0742-1) · 71335-0742-1
- 60 TABLET in 1 BOTTLE (71335-0742-2) · 71335-0742-2
- 90 TABLET in 1 BOTTLE (71335-0742-3) · 71335-0742-3
- 18 TABLET in 1 BOTTLE (71335-0742-4) · 71335-0742-4
- 100 TABLET in 1 BOTTLE (71335-0742-5) · 71335-0742-5
- 45 TABLET in 1 BOTTLE (71335-0742-6) · 71335-0742-6
- 180 TABLET in 1 BOTTLE (71335-0742-7) · 71335-0742-7
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 →