hydroxyzine hydrochloride
Generic: hydroxyzine hydrochloride
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
hydroxyzine hydrochloride
Generic Name
hydroxyzine hydrochloride
Labeler
a-s medication solutions
Dosage Form
TABLET
Routes
Active Ingredients
hydroxyzine dihydrochloride 25 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50090-6626
Product ID
50090-6626_3aa1348c-dc6e-4500-abdc-9170862a52c5
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA040840
Listing Expiration
2026-12-31
Marketing Start
2009-11-11
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500906626
Hyphenated Format
50090-6626
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
- 90 TABLET in 1 BOTTLE (50090-6626-0)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3aa1348c-dc6e-4500-abdc-9170862a52c5", "openfda": {"unii": ["76755771U3"], "rxcui": ["995258"], "spl_set_id": ["46266803-0905-4ae2-9d17-dbf4c2a08181"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-6626-0)", "package_ndc": "50090-6626-0", "marketing_start_date": "20230825"}], "brand_name": "HydrOXYzine Hydrochloride", "product_id": "50090-6626_3aa1348c-dc6e-4500-abdc-9170862a52c5", "dosage_form": "TABLET", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "50090-6626", "generic_name": "HydrOXYzine Hydrochloride", "labeler_name": "A-S Medication Solutions", "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_start_date": "20091111", "listing_expiration_date": "20261231"}