Package 43063-518-28

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 43063-518-28
Digits Only 4306351828
Product NDC 43063-518
Description

28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-518-28)

Marketing

Marketing Status
Marketed Since 2012-07-24
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": "4138e4f8-23cf-c563-e063-6294a90ad9bb", "openfda": {"unii": ["76755771U3"], "rxcui": ["995258"], "spl_set_id": ["24cb9c83-a7e4-4bae-997c-c3a87426f78c"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-518-06)", "package_ndc": "43063-518-06", "marketing_start_date": "20120724"}, {"sample": false, "description": "12 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-518-12)", "package_ndc": "43063-518-12", "marketing_start_date": "20120724"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-518-20)", "package_ndc": "43063-518-20", "marketing_start_date": "20120724"}, {"sample": false, "description": "28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-518-28)", "package_ndc": "43063-518-28", "marketing_start_date": "20120724"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-518-30)", "package_ndc": "43063-518-30", "marketing_start_date": "20120724"}, {"sample": false, "description": "40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-518-40)", "package_ndc": "43063-518-40", "marketing_start_date": "20120724"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-518-60)", "package_ndc": "43063-518-60", "marketing_start_date": "20191218"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-518-90)", "package_ndc": "43063-518-90", "marketing_start_date": "20120724"}], "brand_name": "Hydroxyzine Hydrochloride", "product_id": "43063-518_4138e4f8-23cf-c563-e063-6294a90ad9bb", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "43063-518", "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": "25 mg/1"}], "application_number": "ANDA040787", "marketing_category": "ANDA", "marketing_start_date": "20120724", "listing_expiration_date": "20261231"}