Package 71205-332-90

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 71205-332-90
Digits Only 7120533290
Product NDC 71205-332
Product ID 71205-332_543de8c8-ee2a-4cdc-8968-5fba573d7ebe
Description

90 TABLET, FILM COATED in 1 BOTTLE (71205-332-90)

Marketing

Marketing Status
Marketed Since 2019-09-01
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": "543de8c8-ee2a-4cdc-8968-5fba573d7ebe", "openfda": {"unii": ["76755771U3"], "rxcui": ["995281"], "spl_set_id": ["3edfac5c-a08b-4270-a343-9b2dc10a4a6e"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET, FILM COATED in 1 BOTTLE (71205-332-15)", "package_ndc": "71205-332-15", "marketing_start_date": "20190901"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (71205-332-20)", "package_ndc": "71205-332-20", "marketing_start_date": "20190901"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71205-332-30)", "package_ndc": "71205-332-30", "marketing_start_date": "20190901"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71205-332-60)", "package_ndc": "71205-332-60", "marketing_start_date": "20190901"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71205-332-90)", "package_ndc": "71205-332-90", "marketing_start_date": "20190901"}], "brand_name": "Hydroxyzine Hydrochloride", "product_id": "71205-332_543de8c8-ee2a-4cdc-8968-5fba573d7ebe", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "71205-332", "generic_name": "Hydroxyzine Hydrochloride", "labeler_name": "Proficient Rx LP", "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"}