Package 83745-232-16

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 83745-232-16
Digits Only 8374523216
Product NDC 83745-232
Description

473 mL in 1 BOTTLE (83745-232-16)

Marketing

Marketing Status
Marketed Since 2024-07-16
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": "832542b8-0454-465e-a50d-a749dcd1a84d", "openfda": {"upc": ["0383745232166"], "unii": ["76755771U3"], "rxcui": ["995241"], "spl_set_id": ["87d4bbff-0498-4c26-86cb-7ce173afa0b6"], "manufacturer_name": ["APOZEAL PHARMACEUTICALS INC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "473 mL in 1 BOTTLE (83745-232-16)", "package_ndc": "83745-232-16", "marketing_start_date": "20240716"}], "brand_name": "HYDROXYZINE HYDROCHLORIDE", "product_id": "83745-232_832542b8-0454-465e-a50d-a749dcd1a84d", "dosage_form": "SOLUTION", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "83745-232", "generic_name": "HYDROXYZINE HYDROCHLORIDE", "labeler_name": "APOZEAL PHARMACEUTICALS INC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HYDROXYZINE HYDROCHLORIDE", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "10 mg/5mL"}], "application_number": "ANDA210634", "marketing_category": "ANDA", "marketing_start_date": "20240716", "listing_expiration_date": "20271231"}