Nefazodone Hydrochloride

Product NDC
63629-7310
11-digit product format
636297310
Labeler code
63629
Product ID
63629-7310_498ea1ce-c77a-4a4d-9d1f-ea7bd58a92a9
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Nefazodone Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA076037
Marketing category
ANDA
Marketing start
2003-09-16
Marketing end
0000-00-00
Substance
NEFAZODONE HYDROCHLORIDE
Active strength
200 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

FDA-Initiated Inactive NDC Indexing#

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
63629-7310-16362973100130 TABLET in 1 BOTTLE (63629-7310-1) 30 tablet2017-06-130000-00-00NoNoCurrent
63629-7310-26362973100228 TABLET in 1 BOTTLE (63629-7310-2) 28 tablet2017-06-130000-00-00NoNoCurrent
63629-7310-36362973100390 TABLET in 1 BOTTLE (63629-7310-3) 90 tablet2017-06-130000-00-00NoNoCurrent
63629-7310-46362973100460 TABLET in 1 BOTTLE (63629-7310-4) 60 tablet2017-06-130000-00-00NoNoCurrent