Package 68071-4499-3

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-4499-3
Digits Only 6807144993
Product NDC 68071-4499
Product ID 68071-4499_1a8d9b76-64fd-adfb-e063-6394a90aafa0
Description

30 TABLET, FILM COATED in 1 BOTTLE (68071-4499-3)

Marketing

Marketing Status
Marketed Since 2018-07-18
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": "1a8d9b76-64fd-adfb-e063-6394a90aafa0", "openfda": {"upc": ["0368071449938"], "unii": ["76755771U3"], "rxcui": ["995218"], "spl_set_id": ["714a26a1-371f-ef23-e053-2a95a90a6af6"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68071-4499-3)", "package_ndc": "68071-4499-3", "marketing_start_date": "20180718"}], "brand_name": "Hydroxyzine Hydrochloride", "product_id": "68071-4499_1a8d9b76-64fd-adfb-e063-6394a90aafa0", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "68071-4499", "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": "10 mg/1"}], "application_number": "ANDA088617", "marketing_category": "ANDA", "marketing_start_date": "20130219", "listing_expiration_date": "20261231"}