Package 68071-5286-3

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-5286-3
Digits Only 6807152863
Product NDC 68071-5286
Product ID 68071-5286_1d7925ca-b449-bc0f-e063-6394a90ad4d3
Description

30 TABLET in 1 BOTTLE (68071-5286-3)

Marketing

Marketing Status
Marketed Since 2020-06-22
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": "1d7925ca-b449-bc0f-e063-6394a90ad4d3", "openfda": {"upc": ["0368071528633"], "unii": ["76755771U3"], "rxcui": ["995258"], "spl_set_id": ["a8af7dd0-fef8-5c39-e053-2a95a90ae11a"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-5286-3)", "package_ndc": "68071-5286-3", "marketing_start_date": "20200622"}], "brand_name": "Hydroxyzine hydrochloride", "product_id": "68071-5286_1d7925ca-b449-bc0f-e063-6394a90ad4d3", "dosage_form": "TABLET", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "68071-5286", "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": "ANDA204279", "marketing_category": "ANDA", "marketing_start_date": "20140820", "listing_expiration_date": "20261231"}