Package 0404-9878-02

Brand: hydroxyzine

Generic: hydroxyzine
NDC Package

Package Facts

Identity

Package NDC 0404-9878-02
Digits Only 0404987802
Product NDC 0404-9878
Description

1 VIAL, SINGLE-DOSE in 1 BAG (0404-9878-02) / 2 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2022-01-17
Brand hydroxyzine
Generic hydroxyzine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR"], "spl_id": "5d9b6c38-5a58-4278-999a-f430f34aafd4", "openfda": {"unii": ["76755771U3"], "rxcui": ["1794552"], "spl_set_id": ["851e7439-bb0a-4a09-9279-e3c33bff8965"], "manufacturer_name": ["Henry Schein, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 BAG (0404-9878-02)  / 2 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "0404-9878-02", "marketing_start_date": "20220117"}], "brand_name": "Hydroxyzine", "product_id": "0404-9878_5d9b6c38-5a58-4278-999a-f430f34aafd4", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "0404-9878", "generic_name": "Hydroxyzine", "labeler_name": "Henry Schein, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxyzine", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "50 mg/mL"}], "application_number": "ANDA087408", "marketing_category": "ANDA", "marketing_start_date": "20220117", "listing_expiration_date": "20261231"}