Package 16714-081-11

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 16714-081-11
Digits Only 1671408111
Product NDC 16714-081
Product ID 16714-081_1a8febc0-9d51-4026-8ea6-6cba69e841c5
Description

500 TABLET in 1 BOTTLE (16714-081-11)

Marketing

Marketing Status
Marketed Since 2009-11-11
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": "1a8febc0-9d51-4026-8ea6-6cba69e841c5", "openfda": {"upc": ["0316714081106", "0316714082103", "0316714083100"], "unii": ["76755771U3"], "rxcui": ["995218", "995258", "995281"], "spl_set_id": ["8e5fce17-936e-46ea-a969-518c952c2091"], "manufacturer_name": ["Northstar RxLLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (16714-081-10)", "package_ndc": "16714-081-10", "marketing_start_date": "20091111"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (16714-081-11)", "package_ndc": "16714-081-11", "marketing_start_date": "20091111"}], "brand_name": "HydrOXYzine Hydrochloride", "product_id": "16714-081_1a8febc0-9d51-4026-8ea6-6cba69e841c5", "dosage_form": "TABLET", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "16714-081", "generic_name": "HydrOXYzine Hydrochloride", "labeler_name": "Northstar RxLLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HydrOXYzine Hydrochloride", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA040840", "marketing_category": "ANDA", "marketing_start_date": "20091111", "listing_expiration_date": "20271231"}