Package 72789-269-30

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 72789-269-30
Digits Only 7278926930
Product NDC 72789-269
Product ID 72789-269_3caaf087-bb2f-80b0-e063-6294a90a1cfc
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-269-30)

Marketing

Marketing Status
Marketed Since 2022-08-16
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": "3caaf087-bb2f-80b0-e063-6294a90a1cfc", "openfda": {"upc": ["0372789269306"], "unii": ["76755771U3"], "rxcui": ["995281"], "spl_set_id": ["214b3f14-2f6c-4f36-b7a6-e0b1f820e3a7"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-269-30)", "package_ndc": "72789-269-30", "marketing_start_date": "20220816"}], "brand_name": "Hydroxyzine Hydrochloride", "product_id": "72789-269_3caaf087-bb2f-80b0-e063-6294a90a1cfc", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "72789-269", "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": "ANDA088619", "marketing_category": "ANDA", "marketing_start_date": "20121022", "listing_expiration_date": "20261231"}