Package 68071-4622-3

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-4622-3
Digits Only 6807146223
Product NDC 68071-4622
Product ID 68071-4622_22fa4098-a077-b528-e063-6394a90abbe7
Description

30 TABLET, FILM COATED in 1 BOTTLE (68071-4622-3)

Marketing

Marketing Status
Marketed Since 2018-11-05
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": "22fa4098-a077-b528-e063-6394a90abbe7", "openfda": {"upc": ["0368071462234"], "unii": ["76755771U3"], "rxcui": ["995258"], "spl_set_id": ["79f38cc2-f72f-3f30-e053-2991aa0ac540"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68071-4622-3)", "package_ndc": "68071-4622-3", "marketing_start_date": "20181105"}], "brand_name": "Hydroxyzine Hydrochloride", "product_id": "68071-4622_22fa4098-a077-b528-e063-6394a90abbe7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "68071-4622", "generic_name": "Hydroxyzine Hydrochloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxyzine Hydrochloride", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "25 mg/1"}], "application_number": "ANDA040602", "marketing_category": "ANDA", "marketing_start_date": "20150331", "listing_expiration_date": "20261231"}