Package 63187-733-30

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63187-733-30
Digits Only 6318773330
Product NDC 63187-733
Description

30 TABLET in 1 BOTTLE (63187-733-30)

Marketing

Marketing Status
Marketed Since 2016-07-01
Brand hydroxyzine hydrochloride
Generic hydroxyzine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "edabc25f-0f5d-42c1-8edc-b3e5bcc4dd45", "openfda": {"upc": ["0363187733308"], "unii": ["76755771U3"], "rxcui": ["995258"], "spl_set_id": ["83e8d60d-36fd-4223-b50c-e6615045352a"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET in 1 BOTTLE (63187-733-20)", "package_ndc": "63187-733-20", "marketing_start_date": "20170102"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (63187-733-30)", "package_ndc": "63187-733-30", "marketing_start_date": "20160701"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (63187-733-60)", "package_ndc": "63187-733-60", "marketing_start_date": "20160701"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (63187-733-90)", "package_ndc": "63187-733-90", "marketing_start_date": "20160701"}], "brand_name": "Hydroxyzine hydrochloride", "product_id": "63187-733_edabc25f-0f5d-42c1-8edc-b3e5bcc4dd45", "dosage_form": "TABLET", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "63187-733", "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": "25 mg/1"}], "application_number": "ANDA204279", "marketing_category": "ANDA", "marketing_start_date": "20120324", "listing_expiration_date": "20261231"}