Package 59651-793-99

Brand: haloperidol

Generic: haloperidol
NDC Package

Package Facts

Identity

Package NDC 59651-793-99
Digits Only 5965179399
Product NDC 59651-793
Description

1000 TABLET in 1 BOTTLE (59651-793-99)

Marketing

Marketing Status
Marketed Since 2024-04-19
Brand haloperidol
Generic haloperidol
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "265a70c4-9b29-464c-9258-735bd2b2ccf7", "openfda": {"nui": ["N0000180182"], "unii": ["J6292F8L3D"], "rxcui": ["197754", "310670", "310671", "310672", "314034", "314035"], "spl_set_id": ["bf21633e-f37b-4017-a143-538eb005de2d"], "pharm_class_epc": ["Typical Antipsychotic [EPC]"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (59651-793-01)", "package_ndc": "59651-793-01", "marketing_start_date": "20240419"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (59651-793-99)", "package_ndc": "59651-793-99", "marketing_start_date": "20240419"}], "brand_name": "Haloperidol", "product_id": "59651-793_265a70c4-9b29-464c-9258-735bd2b2ccf7", "dosage_form": "TABLET", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "59651-793", "generic_name": "Haloperidol", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Haloperidol", "active_ingredients": [{"name": "HALOPERIDOL", "strength": "10 mg/1"}], "application_number": "ANDA218789", "marketing_category": "ANDA", "marketing_start_date": "20240419", "listing_expiration_date": "20261231"}