Package 10702-012-50

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 10702-012-50
Digits Only 1070201250
Product NDC 10702-012
Product ID 10702-012_eff46bea-a884-5878-e053-2a95a90ae664
Description

500 TABLET, FILM COATED in 1 BOTTLE (10702-012-50)

Marketing

Marketing Status
Marketed Since 2012-07-24
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": "eff46bea-a884-5878-e053-2a95a90ae664", "openfda": {"upc": ["0310702012103"], "unii": ["76755771U3"], "rxcui": ["995218", "995258", "995281"], "spl_set_id": ["adc4cb73-77c6-48ff-aaf2-b3568d53de1f"], "manufacturer_name": ["KVK-Tech, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (10702-012-01)", "package_ndc": "10702-012-01", "marketing_start_date": "20120724"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (10702-012-10)", "package_ndc": "10702-012-10", "marketing_start_date": "20120724"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (10702-012-50)", "package_ndc": "10702-012-50", "marketing_start_date": "20120724"}], "brand_name": "Hydroxyzine Hydrochloride", "product_id": "10702-012_eff46bea-a884-5878-e053-2a95a90ae664", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "10702-012", "generic_name": "Hydroxyzine Hydrochloride", "labeler_name": "KVK-Tech, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxyzine Hydrochloride", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA040786", "marketing_category": "ANDA", "marketing_start_date": "20120724", "listing_expiration_date": "20261231"}