Package 76420-882-30

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 76420-882-30
Digits Only 7642088230
Product NDC 76420-882
Product ID 76420-882_2979cc3d-941b-4936-e063-6394a90ab8f8
Description

30 TABLET in 1 BOTTLE (76420-882-30)

Marketing

Marketing Status
Marketed Since 2024-12-17
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": "2979cc3d-941b-4936-e063-6394a90ab8f8", "openfda": {"unii": ["76755771U3"], "rxcui": ["995218", "995258", "995281"], "spl_set_id": ["4f3266f4-00a6-4c0c-bff2-e606913de894"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (76420-882-01)", "package_ndc": "76420-882-01", "marketing_start_date": "20241217"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (76420-882-05)", "package_ndc": "76420-882-05", "marketing_start_date": "20241217"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (76420-882-10)", "package_ndc": "76420-882-10", "marketing_start_date": "20241217"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (76420-882-30)", "package_ndc": "76420-882-30", "marketing_start_date": "20241217"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (76420-882-60)", "package_ndc": "76420-882-60", "marketing_start_date": "20241217"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (76420-882-90)", "package_ndc": "76420-882-90", "marketing_start_date": "20241217"}], "brand_name": "Hydroxyzine hydrochloride", "product_id": "76420-882_2979cc3d-941b-4936-e063-6394a90ab8f8", "dosage_form": "TABLET", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "76420-882", "generic_name": "Hydroxyzine hydrochloride", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxyzine hydrochloride", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA204279", "marketing_category": "ANDA", "marketing_start_date": "20140820", "listing_expiration_date": "20261231"}