Package 60687-664-01

Brand: hydroxyzine hydrochloride

Generic: hydroxyzine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 60687-664-01
Digits Only 6068766401
Product NDC 60687-664
Description

100 BLISTER PACK in 1 CARTON (60687-664-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-664-11)

Marketing

Marketing Status
Marketed Since 2022-10-13
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": "21b18b38-063e-eca0-e063-6294a90a6a86", "openfda": {"unii": ["76755771U3"], "rxcui": ["995218", "995258", "995281"], "spl_set_id": ["47bda4fe-ddb7-4140-900a-970373cc7acc"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (60687-664-01)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-664-11)", "package_ndc": "60687-664-01", "marketing_start_date": "20221013"}], "brand_name": "Hydroxyzine Hydrochloride", "product_id": "60687-664_21b18b38-063e-eca0-e063-6294a90a6a86", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antihistamine [EPC]", "Histamine Receptor Antagonists [MoA]"], "product_ndc": "60687-664", "generic_name": "Hydroxyzine Hydrochloride", "labeler_name": "American Health Packaging", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxyzine Hydrochloride", "active_ingredients": [{"name": "HYDROXYZINE DIHYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA088617", "marketing_category": "ANDA", "marketing_start_date": "20221013", "listing_expiration_date": "20261231"}