Package 68382-079-10

Brand: haloperidol

Generic: haloperidol
NDC Package

Package Facts

Identity

Package NDC 68382-079-10
Digits Only 6838207910
Product NDC 68382-079
Product ID 68382-079_8d46c061-97af-4b2c-a788-bb08031d2c6f
Description

1000 TABLET in 1 BOTTLE (68382-079-10)

Marketing

Marketing Status
Marketed Since 2008-01-03
Brand haloperidol
Generic haloperidol
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "8d46c061-97af-4b2c-a788-bb08031d2c6f", "openfda": {"nui": ["N0000180182"], "upc": ["0368382409010", "0368382080011", "0368382408013"], "unii": ["J6292F8L3D"], "rxcui": ["197754", "310670", "310671", "310672", "314034", "314035"], "spl_set_id": ["54502f78-7244-454a-9171-4e73127f1456"], "pharm_class_epc": ["Typical Antipsychotic [EPC]"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68382-079-01)", "package_ndc": "68382-079-01", "marketing_start_date": "20080103"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (68382-079-10)", "package_ndc": "68382-079-10", "marketing_start_date": "20080103"}], "brand_name": "Haloperidol", "product_id": "68382-079_8d46c061-97af-4b2c-a788-bb08031d2c6f", "dosage_form": "TABLET", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "68382-079", "generic_name": "Haloperidol", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Haloperidol", "active_ingredients": [{"name": "HALOPERIDOL", "strength": "5 mg/1"}], "application_number": "ANDA077580", "marketing_category": "ANDA", "marketing_start_date": "20080103", "listing_expiration_date": "20261231"}