Package 43063-519-30

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 43063-519-30
Digits Only 4306351930
Product NDC 43063-519
Product ID 43063-519_4138e87f-3fda-bee4-e063-6294a90afa2b
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-519-30)

Marketing

Marketing Status
Marketed Since 2012-07-25
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": "4138e87f-3fda-bee4-e063-6294a90afa2b", "openfda": {"upc": ["0343063519301"], "unii": ["76755771U3"], "rxcui": ["995281"], "spl_set_id": ["263d3f22-a105-4abb-8152-be2081eefcde"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-519-30)", "package_ndc": "43063-519-30", "marketing_start_date": "20120725"}], "brand_name": "Hydroxyzine Hydrochloride", "product_id": "43063-519_4138e87f-3fda-bee4-e063-6294a90afa2b", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "43063-519", "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"}