Package 0404-9877-01

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0404-9877-01
Digits Only 0404987701
Product NDC 0404-9877
Description

1 VIAL, SINGLE-DOSE in 1 BAG (0404-9877-01) / 1 mL in 1 VIAL, SINGLE-DOSE

Marketing

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

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR"], "spl_id": "0c90956b-50b1-4f90-97b3-e2f831693504", "openfda": {"unii": ["76755771U3"], "rxcui": ["1794554"], "spl_set_id": ["7279ad5a-0a49-432d-8fa2-17e4c6ecbadc"], "manufacturer_name": ["Henry Schein, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 BAG (0404-9877-01)  / 1 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "0404-9877-01", "marketing_start_date": "20220117"}], "brand_name": "Hydroxyzine Hydrochloride", "product_id": "0404-9877_0c90956b-50b1-4f90-97b3-e2f831693504", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "0404-9877", "generic_name": "Hydroxyzine Hydrochloride", "labeler_name": "Henry Schein, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxyzine Hydrochloride", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "50 mg/mL"}], "application_number": "ANDA087408", "marketing_category": "ANDA", "marketing_start_date": "20220117", "listing_expiration_date": "20261231"}