Package 51655-076-54

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 51655-076-54
Digits Only 5165507654
Product NDC 51655-076
Product ID 51655-076_46ddcf32-22fa-3332-e063-6394a90af421
Description

15 TABLET in 1 BOTTLE, PLASTIC (51655-076-54)

Marketing

Marketing Status
Marketed Since 2023-02-27
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": "46ddcf32-22fa-3332-e063-6394a90af421", "openfda": {"unii": ["76755771U3"], "rxcui": ["995218"], "spl_set_id": ["c134195e-a048-530a-e053-2a95a90ad9f8"], "manufacturer_name": ["Northwind Health Company, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (51655-076-52)", "package_ndc": "51655-076-52", "marketing_start_date": "20201020"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE, PLASTIC (51655-076-54)", "package_ndc": "51655-076-54", "marketing_start_date": "20230227"}], "brand_name": "Hydroxyzine hydrochloride", "product_id": "51655-076_46ddcf32-22fa-3332-e063-6394a90af421", "dosage_form": "TABLET", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "51655-076", "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": "10 mg/1"}], "application_number": "ANDA204279", "marketing_category": "ANDA", "marketing_start_date": "20201020", "listing_expiration_date": "20271231"}