Package 62135-750-47

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 62135-750-47
Digits Only 6213575047
Product NDC 62135-750
Description

473 mL in 1 BOTTLE (62135-750-47)

Marketing

Marketing Status
Marketed Since 2023-08-09
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": "25117412-3663-105d-e063-6394a90a0d64", "openfda": {"upc": ["0362135750473"], "unii": ["76755771U3"], "rxcui": ["995241"], "spl_set_id": ["53b2d731-f38a-47c0-9e5c-abd3b45e2fe1"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (62135-750-47)", "package_ndc": "62135-750-47", "marketing_start_date": "20230809"}], "brand_name": "HYDROXYZINE HYDROCHLORIDE", "product_id": "62135-750_25117412-3663-105d-e063-6394a90a0d64", "dosage_form": "SYRUP", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "62135-750", "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": "ANDA087294", "marketing_category": "ANDA", "marketing_start_date": "19820412", "listing_expiration_date": "20261231"}