Package 43063-963-95

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 43063-963-95
Digits Only 4306396395
Product NDC 43063-963
Product ID 43063-963_415f3642-ef05-3671-e063-6294a90ab7a7
Description

1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-963-95)

Marketing

Marketing Status
Marketed Since 2019-04-01
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": "415f3642-ef05-3671-e063-6294a90ab7a7", "openfda": {"upc": ["0343063962954", "0343063963012"], "unii": ["76755771U3"], "rxcui": ["995218", "995258", "995281"], "spl_set_id": ["1a3e389f-391d-4f37-9e34-ce3c6f5fe8c1"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-963-01)", "package_ndc": "43063-963-01", "marketing_start_date": "20190401"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-963-95)", "package_ndc": "43063-963-95", "marketing_start_date": "20190401"}], "brand_name": "Hydroxyzine Hydrochloride", "product_id": "43063-963_415f3642-ef05-3671-e063-6294a90ab7a7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "43063-963", "generic_name": "Hydroxyzine Hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxyzine Hydrochloride", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA040788", "marketing_category": "ANDA", "marketing_start_date": "20120724", "listing_expiration_date": "20261231"}