Package 82619-106-01

Brand: haloperidol

Generic: haloperidol
NDC Package

Package Facts

Identity

Package NDC 82619-106-01
Digits Only 8261910601
Product NDC 82619-106
Product ID 82619-106_46d58435-0437-e206-e063-6294a90ae755
Description

100 TABLET in 1 BOTTLE (82619-106-01)

Marketing

Marketing Status
Marketed Since 2026-01-05
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": "46d58435-0437-e206-e063-6294a90ae755", "openfda": {"nui": ["N0000180182"], "upc": ["0382619105018", "0382619105025", "0382619108033", "0382619109023", "0382619109016", "0382619109030", "0382619110029", "0382619106022", "0382619107029", "0382619106015", "0382619107012", "0382619108026"], "unii": ["J6292F8L3D"], "rxcui": ["197754", "310670", "310671", "310672", "314034", "314035"], "spl_set_id": ["9763c044-7430-48f7-bf3e-da1c7c683955"], "pharm_class_epc": ["Typical Antipsychotic [EPC]"], "manufacturer_name": ["Creekwood Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (82619-106-01)", "package_ndc": "82619-106-01", "marketing_start_date": "20260105"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (82619-106-02)", "package_ndc": "82619-106-02", "marketing_start_date": "20260105"}], "brand_name": "HALOPERIDOL", "product_id": "82619-106_46d58435-0437-e206-e063-6294a90ae755", "dosage_form": "TABLET", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "82619-106", "generic_name": "haloperidol", "labeler_name": "Creekwood Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HALOPERIDOL", "active_ingredients": [{"name": "HALOPERIDOL", "strength": "1 mg/1"}], "application_number": "ANDA218162", "marketing_category": "ANDA", "marketing_start_date": "20260105", "listing_expiration_date": "20261231"}