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
- 71335-1630_71a7289b-e835-441f-9d96-ec5fe8b051b5
- Product NDC
- 71335-1630
- Form
- TABLET
- Composition / generic term
- Trazodone Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20171211 / 20281231
Source-listed ingredients
- TRAZODONE HYDROCHLORIDE — 100 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE (71335-1630-1) · 71335-1630-1
- 60 TABLET in 1 BOTTLE (71335-1630-2) · 71335-1630-2
- 90 TABLET in 1 BOTTLE (71335-1630-3) · 71335-1630-3
- 180 TABLET in 1 BOTTLE (71335-1630-4) · 71335-1630-4
- 28 TABLET in 1 BOTTLE (71335-1630-5) · 71335-1630-5
- 10 TABLET in 1 BOTTLE (71335-1630-6) · 71335-1630-6
- 120 TABLET in 1 BOTTLE (71335-1630-7) · 71335-1630-7
- 45 TABLET in 1 BOTTLE (71335-1630-8) · 71335-1630-8
- 14 TABLET in 1 BOTTLE (71335-1630-9) · 71335-1630-9
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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