Hydroxyzine hydrochloride

Product NDC
66267-499
11-digit product format
662670499
Labeler code
66267
Product ID
66267-499_415c74b0-cdba-54bc-e054-00144ff88e88
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Hydroxyzine hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
NuCare Pharmaceuticals, Inc.
Application
ANDA204279
Marketing category
ANDA
Marketing start
2012-03-24
Marketing end
0000-00-00
Substance
HYDROXYZINE HYDROCHLORIDE
Active strength
50 mg/1
Pharmacologic classes
Antihistamine [EPC],Histamine Receptor Antagonists [MoA]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
66267-499-602020-03-06C16284748780-19d75b9d0-9d48-f424-e053-dadaa90a57ce415c74b0-cdb9-54bc-e054-00144ff88e88
66267-499-602020-01-31C16284748780-19d75b9d0-9d48-f424-e053-dadaa90a57ce415c74b0-cdb9-54bc-e054-00144ff88e88