Trazodone Hydrochloride

Product NDC
71335-0705
11-digit product format
713350705
Labeler code
71335
Product ID
71335-0705_37651ec2-0d18-3c66-e063-6294a90afbdb
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Trazodone Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
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
71335-0705-07133507050014 TABLET in 1 BOTTLE (71335-0705-0) 14 tablet2019-08-12NoNoHistorical
71335-0705-17133507050120 TABLET in 1 BOTTLE (71335-0705-1) 20 tablet2020-02-14NoNoHistorical
71335-0705-27133507050230 TABLET in 1 BOTTLE (71335-0705-2) 30 tablet2018-03-14NoNoHistorical
71335-0705-37133507050360 TABLET in 1 BOTTLE (71335-0705-3) 60 tablet2018-03-07NoNoHistorical
71335-0705-47133507050490 TABLET in 1 BOTTLE (71335-0705-4) 90 tablet2018-02-28NoNoHistorical
71335-0705-57133507050545 TABLET in 1 BOTTLE (71335-0705-5) 45 tablet2025-06-11NoNoHistorical
71335-0705-671335070506100 TABLET in 1 BOTTLE (71335-0705-6) 100 tablet2018-05-31NoNoHistorical
71335-0705-77133507050725 TABLET in 1 BOTTLE (71335-0705-7) 25 tablet2025-06-11NoNoHistorical
71335-0705-871335070508120 TABLET in 1 BOTTLE (71335-0705-8) 120 tablet2020-02-26NoNoHistorical
71335-0705-97133507050928 TABLET in 1 BOTTLE (71335-0705-9) 28 tablet2025-06-11NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Trazodone HydrochlorideBryant Ranch Prepack2025-06-12HUMAN PRESCRIPTION DRUG LABEL13