Package 71335-3036-1

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71335-3036-1
Digits Only 7133530361
Product NDC 71335-3036
Product ID 71335-3036_52f79423-8a65-411f-b83b-e314df3811c1
Description

1000 TABLET, FILM COATED in 1 BOTTLE (71335-3036-1)

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": "52f79423-8a65-411f-b83b-e314df3811c1", "openfda": {"unii": ["76755771U3"], "rxcui": ["995281"], "spl_set_id": ["3526a66b-2182-4b5a-a7d1-563d75f5335f"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (71335-3036-1)", "package_ndc": "71335-3036-1", "marketing_start_date": "20251203"}], "brand_name": "Hydroxyzine Hydrochloride", "product_id": "71335-3036_52f79423-8a65-411f-b83b-e314df3811c1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "71335-3036", "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": "50 mg/1"}], "application_number": "ANDA087871", "marketing_category": "ANDA", "marketing_start_date": "20211007", "listing_expiration_date": "20261231"}