Trazodone Hydrochloride

Product NDC
66267-392
11-digit product format
662670392
Labeler code
66267
Product ID
66267-392_9cbd33ff-eec7-488d-e053-2a95a90a9202
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Trazodone Hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
NuCare Pharmaceuticals, Inc.
Application
ANDA072192
Marketing category
ANDA
Marketing start
2010-05-30
Marketing end
0000-00-00
Substance
TRAZODONE HYDROCHLORIDE
Active strength
100 mg/1
Pharmacologic classes
Serotonin Reuptake Inhibitor [EPC]
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
66267-392-30EA - Each66267-392eac3d9bf-824c-4382-a391-e1bdfccba4dd12017-03-06
66267-392-60EA - Each66267-392ee2fe81d-0a23-4665-86bd-13cce4e0cf0012017-03-06