Package 35573-442-02

Brand: HALOPERIDOL

Generic: HALOPERIDOL
NDC Package

Package Facts

Identity

Package NDC 35573-442-02
Digits Only 3557344202
Product NDC 35573-442
Product ID 35573-442_941ba97a-5024-4579-98e3-5fad0a5c1c37
Description

100 TABLET in 1 BOTTLE (35573-442-02)

Marketing

Marketing Status
Discontinued 2026-02-28
Brand HALOPERIDOL
Generic HALOPERIDOL
Sample Package No

Linked Drug Pages (1)

HALOPERIDOL ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "941ba97a-5024-4579-98e3-5fad0a5c1c37", "openfda": {"nui": ["N0000180182"], "unii": ["J6292F8L3D"], "rxcui": ["314035"], "spl_set_id": ["43bb14ed-d0c3-43be-92c4-ccb913737390"], "pharm_class_epc": ["Typical Antipsychotic [EPC]"], "manufacturer_name": ["Burel Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (35573-442-02)", "package_ndc": "35573-442-02", "marketing_end_date": "20260228", "marketing_start_date": "20210531"}], "brand_name": "HALOPERIDOL", "product_id": "35573-442_941ba97a-5024-4579-98e3-5fad0a5c1c37", "dosage_form": "TABLET", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "35573-442", "generic_name": "HALOPERIDOL", "labeler_name": "Burel Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HALOPERIDOL", "active_ingredients": [{"name": "HALOPERIDOL", "strength": "10 mg/1"}], "application_number": "ANDA071132", "marketing_category": "ANDA", "marketing_end_date": "20260228", "marketing_start_date": "20210531"}