Package 35573-441-02

Brand: HALOPERIDOL

Generic: HALOPERIDOL
NDC Package

Package Facts

Identity

Package NDC 35573-441-02
Digits Only 3557344102
Product NDC 35573-441
Product ID 35573-441_e2f75686-47b4-4043-a5eb-b26d93f7b15a
Description

100 TABLET in 1 BOTTLE (35573-441-02)

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": "e2f75686-47b4-4043-a5eb-b26d93f7b15a", "openfda": {"nui": ["N0000180182"], "unii": ["J6292F8L3D"], "rxcui": ["310672"], "spl_set_id": ["7a71f18a-3a8c-4adb-8adf-660fcd8bf9b3"], "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 (35573-441-02)", "package_ndc": "35573-441-02", "marketing_end_date": "20260228", "marketing_start_date": "20210531"}], "brand_name": "HALOPERIDOL", "product_id": "35573-441_e2f75686-47b4-4043-a5eb-b26d93f7b15a", "dosage_form": "TABLET", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "35573-441", "generic_name": "HALOPERIDOL", "labeler_name": "Burel Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HALOPERIDOL", "active_ingredients": [{"name": "HALOPERIDOL", "strength": "5 mg/1"}], "application_number": "ANDA071131", "marketing_category": "ANDA", "marketing_end_date": "20260228", "marketing_start_date": "20210531"}