Package 0121-1034-16

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0121-1034-16
Digits Only 0121103416
Product NDC 0121-1034
Product ID 0121-1034_44c48714-8f0c-4628-9783-ff32360b457d
Description

473 mL in 1 BOTTLE (0121-1034-16)

Marketing

Marketing Status
Marketed Since 2024-11-14
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": "44c48714-8f0c-4628-9783-ff32360b457d", "openfda": {"upc": ["0301211034168"], "unii": ["76755771U3"], "rxcui": ["995241"], "spl_set_id": ["2a343906-0bea-4bd8-bd35-c3f199d9b266"], "manufacturer_name": ["PAI Holdings, LLC dba PAI Pharma"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (0121-1034-16)", "package_ndc": "0121-1034-16", "marketing_start_date": "20241114"}], "brand_name": "Hydroxyzine Hydrochloride", "product_id": "0121-1034_44c48714-8f0c-4628-9783-ff32360b457d", "dosage_form": "SOLUTION", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "0121-1034", "generic_name": "hydroxyzine hydrochloride", "labeler_name": "PAI Holdings, LLC dba PAI Pharma", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxyzine Hydrochloride", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "10 mg/5mL"}], "application_number": "ANDA040391", "marketing_category": "ANDA", "marketing_start_date": "20020410", "listing_expiration_date": "20261231"}