Package 71335-3035-1

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-3035-1
Digits Only 7133530351
Product NDC 71335-3035
Product ID 71335-3035_73236eaf-d2da-4b4d-aa43-6c38d71a6ca3
Description

1000 TABLET, FILM COATED in 1 BOTTLE (71335-3035-1)

Marketing

Marketing Status
Marketed Since 2025-12-03
Brand hydroxyzine hydrochloride
Generic hydroxyzine hydrochloride
Sample Package No

Linked Drug Pages (1)

Hydroxyzine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "73236eaf-d2da-4b4d-aa43-6c38d71a6ca3", "openfda": {"unii": ["76755771U3"], "rxcui": ["995258"], "spl_set_id": ["f84e3365-57d2-4904-9275-96600f8d74c7"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (71335-3035-1)", "package_ndc": "71335-3035-1", "marketing_start_date": "20251203"}], "brand_name": "Hydroxyzine Hydrochloride", "product_id": "71335-3035_73236eaf-d2da-4b4d-aa43-6c38d71a6ca3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "71335-3035", "generic_name": "Hydroxyzine Hydrochloride", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxyzine Hydrochloride", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA087871", "marketing_category": "ANDA", "marketing_start_date": "20211007", "listing_expiration_date": "20261231"}