Package 62135-750-47
Brand: hydroxyzine hydrochloride
Generic: hydroxyzine hydrochloridePackage 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
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"}