Package 62135-545-05

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 62135-545-05
Digits Only 6213554505
Product NDC 62135-545
Product ID 62135-545_258a2adf-df42-7a34-e063-6294a90a84ca
Description

500 TABLET, FILM COATED in 1 BOTTLE (62135-545-05)

Marketing

Marketing Status
Marketed Since 2023-06-28
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": "258a2adf-df42-7a34-e063-6294a90a84ca", "openfda": {"upc": ["0362135545055", "0362135545123", "0362135547059", "0362135546052", "0362135546120", "0362135547127"], "unii": ["76755771U3"], "rxcui": ["995218", "995258", "995281"], "spl_set_id": ["934afb42-fee8-415b-8090-2265bb299afe"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (62135-545-05)", "package_ndc": "62135-545-05", "marketing_start_date": "20230628"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (62135-545-12)", "package_ndc": "62135-545-12", "marketing_start_date": "20230628"}], "brand_name": "Hydroxyzine Hydrochloride", "product_id": "62135-545_258a2adf-df42-7a34-e063-6294a90a84ca", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "62135-545", "generic_name": "Hydroxyzine Hydrochloride", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxyzine Hydrochloride", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA040804", "marketing_category": "ANDA", "marketing_start_date": "20080630", "listing_expiration_date": "20261231"}