Hydroxyzine hydrochloride

Product NDC
0615-8037
11-digit product format
006158037
Labeler code
0615
Product ID
0615-8037_120a6264-0f31-4536-884a-1ce5a1805331
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Hydroxyzine hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
NCS HealthCare of KY, Inc dba Vangard Labs
Application
ANDA204279
Marketing category
ANDA
Marketing start
2012-03-24
Marketing end
0000-00-00
Substance
HYDROXYZINE HYDROCHLORIDE
Active strength
25 mg/1
Pharmacologic classes
Antihistamine [EPC],Histamine Receptor Antagonists [MoA]
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0615-8037-392021-06-16C16284748780-19d75b9d0-f220-f424-e053-dadaa90a57ce84fe92eb-ae3c-4f2c-a02c-102596d22350
0615-8037-392020-01-31C16284748780-19d75b9d0-f220-f424-e053-dadaa90a57ce84fe92eb-ae3c-4f2c-a02c-102596d22350