Package 51655-119-52

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51655-119-52
Digits Only 5165511952
Product NDC 51655-119
Product ID 51655-119_499db2fe-4808-e2f7-e063-6394a90ab068
Description

30 TABLET in 1 BOTTLE, PLASTIC (51655-119-52)

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": "499db2fe-4808-e2f7-e063-6394a90ab068", "openfda": {"unii": ["76755771U3"], "rxcui": ["995281"], "spl_set_id": ["f2b3d10f-2599-5b71-e053-2a95a90a54bb"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-119-52)", "package_ndc": "51655-119-52", "marketing_start_date": "20220816"}], "brand_name": "Hydroxyzine hydrochloride", "product_id": "51655-119_499db2fe-4808-e2f7-e063-6394a90ab068", "dosage_form": "TABLET", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "51655-119", "generic_name": "Hydroxyzine hydrochloride", "labeler_name": "Northwind Health Company, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxyzine hydrochloride", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA204279", "marketing_category": "ANDA", "marketing_start_date": "20220816", "listing_expiration_date": "20271231"}