Package 0093-5062-01

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0093-5062-01
Digits Only 0093506201
Product NDC 0093-5062
Product ID 0093-5062_ce53cc7b-dd6d-4a1b-b64b-ca0b45f67512
Description

100 TABLET, FILM COATED in 1 BOTTLE (0093-5062-01)

Marketing

Marketing Status
Marketed Since 2013-03-11
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": "ce53cc7b-dd6d-4a1b-b64b-ca0b45f67512", "openfda": {"unii": ["76755771U3"], "rxcui": ["995218", "995258", "995281"], "spl_set_id": ["80309ec1-e5d5-4454-b8ce-67d7e6805e44"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (0093-5062-01)", "package_ndc": "0093-5062-01", "marketing_start_date": "20130311"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (0093-5062-05)", "package_ndc": "0093-5062-05", "marketing_start_date": "20121022"}], "brand_name": "Hydroxyzine Hydrochloride", "product_id": "0093-5062_ce53cc7b-dd6d-4a1b-b64b-ca0b45f67512", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "0093-5062", "generic_name": "Hydroxyzine Hydrochloride", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxyzine Hydrochloride", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA088619", "marketing_category": "ANDA", "marketing_start_date": "20121022", "listing_expiration_date": "20261231"}