Package 63629-8740-1

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63629-8740-1
Digits Only 6362987401
Product NDC 63629-8740
Product ID 63629-8740_66ed5a5e-f4d8-4fde-acf2-c7f5d453e21c
Description

100 TABLET, FILM COATED in 1 BOTTLE (63629-8740-1)

Marketing

Marketing Status
Marketed Since 2021-08-27
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": "66ed5a5e-f4d8-4fde-acf2-c7f5d453e21c", "openfda": {"unii": ["76755771U3"], "rxcui": ["995258"], "spl_set_id": ["3f90259a-a684-498f-8963-d02eaba2e9db"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (63629-8740-1)", "package_ndc": "63629-8740-1", "marketing_start_date": "20210827"}], "brand_name": "Hydroxyzine Hydrochloride", "product_id": "63629-8740_66ed5a5e-f4d8-4fde-acf2-c7f5d453e21c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "63629-8740", "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": "ANDA088618", "marketing_category": "ANDA", "marketing_start_date": "20121009", "listing_expiration_date": "20261231"}