Package 68071-5133-6

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 68071-5133-6
Digits Only 6807151336
Product NDC 68071-5133
Product ID 68071-5133_248b221c-df3f-dbf8-e063-6294a90a9251
Description

60 TABLET, FILM COATED in 1 BOTTLE (68071-5133-6)

Marketing

Marketing Status
Marketed Since 2019-12-13
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": "248b221c-df3f-dbf8-e063-6294a90a9251", "openfda": {"upc": ["0368071513363"], "unii": ["76755771U3"], "rxcui": ["995281"], "spl_set_id": ["99995bdb-a35f-7753-e053-2995a90a683c"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (68071-5133-3)", "package_ndc": "68071-5133-3", "marketing_start_date": "20241015"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (68071-5133-6)", "package_ndc": "68071-5133-6", "marketing_start_date": "20191213"}], "brand_name": "Hydroxyzine Hydrochloride", "product_id": "68071-5133_248b221c-df3f-dbf8-e063-6294a90a9251", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "68071-5133", "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": "50 mg/1"}], "application_number": "ANDA040604", "marketing_category": "ANDA", "marketing_start_date": "20150331", "listing_expiration_date": "20261231"}