Package 0517-4201-25

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0517-4201-25
Digits Only 0517420125
Product NDC 0517-4201
Description

25 VIAL, SINGLE-DOSE in 1 TRAY (0517-4201-25) / 1 mL in 1 VIAL, SINGLE-DOSE (0517-4201-01)

Marketing

Marketing Status
Marketed Since 1990-09-30
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": "83de333d-1bf1-4168-8614-6bc79c26d5d0", "openfda": {"upc": ["0305174201254", "0305175601251", "0305175602258"], "unii": ["76755771U3"], "rxcui": ["995270", "995285", "1794552", "1794554"], "spl_set_id": ["8af7e5ce-d9d9-44cc-9f2f-4ddbc89e758a"], "manufacturer_name": ["American Regent, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 TRAY (0517-4201-25)  / 1 mL in 1 VIAL, SINGLE-DOSE (0517-4201-01)", "package_ndc": "0517-4201-25", "marketing_start_date": "19900930"}], "brand_name": "Hydroxyzine Hydrochloride", "product_id": "0517-4201_83de333d-1bf1-4168-8614-6bc79c26d5d0", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "0517-4201", "generic_name": "Hydroxyzine Hydrochloride", "labeler_name": "American Regent, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxyzine Hydrochloride", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "25 mg/mL"}], "application_number": "ANDA087408", "marketing_category": "ANDA", "marketing_start_date": "19900930", "listing_expiration_date": "20261231"}