Trazodone Hydrochloride

Product NDC
71610-874
11-digit product format
716100874
Labeler code
71610
Product ID
71610-874_2d3f115e-f1d4-6dba-e063-6294a90a160d
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Trazodone Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Application
ANDA205253
Marketing category
ANDA
Marketing start
2017-12-11
Substance
TRAZODONE HYDROCHLORIDE
Active strength
50 mg/1
Pharmacologic classes
Serotonin Reuptake Inhibitor [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
6E8ZO8LRNMTRAZODONE HYDROCHLORIDE25332-39-2TRAZODONE HYDROCHLORIDE

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
71610-874-307161008743030 TABLET in 1 BOTTLE (71610-874-30) 30 tablet2025-01-29NoNoHistorical
71610-874-537161008745360 TABLET in 1 BOTTLE (71610-874-53) 60 tablet2025-01-29NoNoHistorical
71610-874-607161008746090 TABLET in 1 BOTTLE (71610-874-60) 90 tablet2025-01-29NoNoHistorical
71610-874-8071610087480180 TABLET in 1 BOTTLE (71610-874-80) 180 tablet2025-01-29NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Trazodone HydrochlorideAphena Pharma Solutions - Tennessee, LLC2025-02-03HUMAN PRESCRIPTION DRUG LABEL1