Hydroxyzine Hydrochloride

Product NDC
66267-113
11-digit product format
662670113
Labeler code
66267
Product ID
66267-113_513a3fa4-8f4e-23bb-e054-00144ff88e88
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Hydroxyzine Hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
NuCare Pharmaceuticals, Inc.
Application
ANDA040804
Marketing category
ANDA
Marketing start
2008-06-30
Marketing end
0000-00-00
Substance
HYDROXYZINE HYDROCHLORIDE
Active strength
25 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#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
66267-113-20EA - Each66267-11377ffbabe-1222-4a94-a9e5-777ac05e2d1212016-11-08
66267-113-30EA - Each66267-11314aca5d5-74b4-4c4d-99e2-17d5393323a012016-11-08