Package 62135-502-47

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 62135-502-47
Digits Only 6213550247
Product NDC 62135-502
Description

473 mL in 1 BOTTLE (62135-502-47)

Marketing

Marketing Status
Marketed Since 2022-10-03
Brand hydroxyzine hydrochloride
Generic hydroxyzine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0770c6f3-a76a-819c-e063-6294a90a3cd8", "openfda": {"upc": ["0362135502478"], "unii": ["76755771U3"], "rxcui": ["995241"], "spl_set_id": ["4590101d-7fb2-478b-acc5-bc9bdbb38ca9"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (62135-502-47)", "package_ndc": "62135-502-47", "marketing_start_date": "20221003"}], "brand_name": "Hydroxyzine Hydrochloride", "product_id": "62135-502_0770c6f3-a76a-819c-e063-6294a90a3cd8", "dosage_form": "SOLUTION", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "62135-502", "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/5mL"}], "application_number": "ANDA201674", "marketing_category": "ANDA", "marketing_start_date": "20130821", "listing_expiration_date": "20261231"}