Trazodone Hydrochloride

Product NDC
71335-0035
11-digit product format
713350035
Labeler code
71335
Product ID
71335-0035_b3160ac4-5942-4f03-ab86-7eae70581b71
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Trazodone Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA071258
Marketing category
ANDA
Marketing start
2008-11-17
Marketing end
0000-00-00
Substance
TRAZODONE HYDROCHLORIDE
Active strength
50 mg/1
Pharmacologic classes
Serotonin Reuptake Inhibitor [EPC]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

Related Records

Related UNII Ingredients

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

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71335-0035-07133500350014 TABLET in 1 BOTTLE (71335-0035-0) 14 tablet2021-12-270000-00-00NoNoCurrent
71335-0035-17133500350120 TABLET in 1 BOTTLE (71335-0035-1) 20 tablet2021-12-270000-00-00NoNoCurrent
71335-0035-27133500350230 TABLET in 1 BOTTLE (71335-0035-2) 30 tablet2021-12-270000-00-00NoNoCurrent
71335-0035-37133500350360 TABLET in 1 BOTTLE (71335-0035-3) 60 tablet2021-12-270000-00-00NoNoCurrent
71335-0035-47133500350490 TABLET in 1 BOTTLE (71335-0035-4) 90 tablet2021-12-270000-00-00NoNoCurrent
71335-0035-57133500350545 TABLET in 1 BOTTLE (71335-0035-5) 45 tablet2021-12-270000-00-00NoNoCurrent
71335-0035-671335003506100 TABLET in 1 BOTTLE (71335-0035-6) 100 tablet2021-12-270000-00-00NoNoCurrent
71335-0035-77133500350725 TABLET in 1 BOTTLE (71335-0035-7) 25 tablet2021-12-270000-00-00NoNoCurrent
71335-0035-871335003508120 TABLET in 1 BOTTLE (71335-0035-8) 120 tablet2021-12-270000-00-00NoNoCurrent
71335-0035-97133500350928 TABLET in 1 BOTTLE (71335-0035-9) 28 tablet2021-12-270000-00-00NoNoCurrent