hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride

Labeler: mckesson corporation dba sky packaging
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name hydroxyzine hydrochloride
Generic Name hydroxyzine hydrochloride
Labeler mckesson corporation dba sky packaging
Dosage Form TABLET
Routes
ORAL
Active Ingredients

hydroxyzine dihydrochloride 25 mg/1

Manufacturer
McKesson Corporation dba SKY Packaging

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
antihistamine [epc] histamine receptor antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63739486
Hyphenated Format 63739-486

Supplemental Identifiers

RxCUI
995218 995258
UNII
76755771U3

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 mg/1
source: ndc
Packaging
  • 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-486-10) / 10 TABLET in 1 BLISTER PACK
source: ndc

Packages (1)

Ingredients (1)

hydroxyzine dihydrochloride (25 mg/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"}