Package 51662-1649-3

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51662-1649-3
Digits Only 5166216493
Product NDC 51662-1649
Description

25 POUCH in 1 CASE (51662-1649-3) / 1 VIAL, MULTI-DOSE in 1 POUCH (51662-1649-2) / 10 mL in 1 VIAL, MULTI-DOSE

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": "19869100-35c6-c014-e063-6294a90a4f11", "openfda": {"unii": ["76755771U3"], "rxcui": ["995270"], "spl_set_id": ["16a63845-6619-293b-e063-6394a90a0a5c"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "25 POUCH in 1 CASE (51662-1649-3)  / 1 VIAL, MULTI-DOSE in 1 POUCH (51662-1649-2)  / 10 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "51662-1649-3", "marketing_start_date": "19900930"}], "brand_name": "HYDROXYZINE HYDROCHLORIDE", "product_id": "51662-1649_19869100-35c6-c014-e063-6294a90a4f11", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "51662-1649", "generic_name": "HYDROXYZINE HYDROCHLORIDE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "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"}