Hydroxyzine

Product NDC
0615-1527
11-digit product format
006151527
Labeler code
0615
Product ID
0615-1527_b6d71446-c2be-4930-8dcf-bb6690512c2a
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Hydroxyzine Hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
NCS HealthCare of KY, Inc dba Vangard Labs
Application
ANDA040786
Marketing category
ANDA
Marketing start
2007-03-20
Marketing end
0000-00-00
Substance
HYDROXYZINE HYDROCHLORIDE
Active strength
50 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
0615-1527-392021-06-16C16284748780-19d75b9d0-b164-f424-e053-dadaa90a57ce367f5dab-95c0-4025-b578-c40e79a7c4f6
0615-1527-392020-01-31C16284748780-19d75b9d0-b164-f424-e053-dadaa90a57ce367f5dab-95c0-4025-b578-c40e79a7c4f6