hydroxyzine hydrochloride
Generic: hydroxyzine hydrochloride
Labeler: mckesson corporation dba sky packagingDrug Facts
Product Profile
Brand Name
hydroxyzine hydrochloride
Generic Name
hydroxyzine hydrochloride
Labeler
mckesson corporation dba sky packaging
Dosage Form
TABLET
Routes
Active Ingredients
hydroxyzine dihydrochloride 25 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
63739-486
Product ID
63739-486_2a322ac0-a904-577c-e063-6294a90acd95
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA040840
Marketing Start
2009-11-11
Marketing End
2026-04-30
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
63739486
Hyphenated Format
63739-486
Supplemental Identifiers
RxCUI
UNII
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
hydroxyzine hydrochloride (source: ndc)
Generic Name
hydroxyzine hydrochloride (source: ndc)
Application Number
ANDA040840 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 mg/1
Packaging
- 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-486-10) / 10 TABLET in 1 BLISTER PACK
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2a322ac0-a904-577c-e063-6294a90acd95", "openfda": {"unii": ["76755771U3"], "rxcui": ["995218", "995258"], "spl_set_id": ["7fff369e-efd8-45c7-bc2b-ca8b623fe716"], "manufacturer_name": ["McKesson Corporation dba SKY Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-486-10) / 10 TABLET in 1 BLISTER PACK", "package_ndc": "63739-486-10", "marketing_end_date": "20260430", "marketing_start_date": "20110303"}], "brand_name": "HydrOXYzine Hydrochloride", "product_id": "63739-486_2a322ac0-a904-577c-e063-6294a90acd95", "dosage_form": "TABLET", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "63739-486", "generic_name": "HydrOXYzine Hydrochloride", "labeler_name": "McKesson Corporation dba SKY Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HydrOXYzine Hydrochloride", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA040840", "marketing_category": "ANDA", "marketing_end_date": "20260430", "marketing_start_date": "20091111"}