Trazodone Hydrochloride

Product NDC
53489-510
11-digit product format
534890510
Labeler code
53489
Product ID
53489-510_a4387b4a-d4d2-48b6-bd6d-e22b69547263
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Trazodone Hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Sun Pharmaceutical Industries, Inc.
Application
ANDA073137
Marketing category
ANDA
Marketing start
1993-03-24
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
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
ac7a3d9b-58c0-4ffc-a3eb-ed863453525eProduct name120250730
b2f15d64-48ea-ba98-af5c-91f410667b31Product name520250314
d8e7f61b-4ab5-0dbe-2706-4e11b6079b87Product name120140508

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
53489-510-01EA - Each53489-5108c2e55f9-09e2-4be9-8310-174f0dea54c312012-07-24

DailyMed Socrata Ingredients#

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
856377traZODone HCl 50 MG Oral TabletPSN9426f88d-2f3f-4dc9-ba17-f4bc0be919631
856377trazodone hydrochloride 50 MG Oral TabletSCD9426f88d-2f3f-4dc9-ba17-f4bc0be919631

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
53489-510-0153489051001100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-510-01) 1993-03-240000-00-00NoNoCurrent
53489-510-075348905100730 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-510-07) 1993-03-240000-00-00NoNoCurrent