Package 69292-582-01

Brand: haloperidol

Generic: haloperidol
NDC Package

Package Facts

Identity

Package NDC 69292-582-01
Digits Only 6929258201
Product NDC 69292-582
Product ID 69292-582_8c9cdd3d-9751-404a-9ceb-276e8dfa6391
Description

100 TABLET in 1 BOTTLE (69292-582-01)

Marketing

Marketing Status
Marketed Since 2022-04-18
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": "8c9cdd3d-9751-404a-9ceb-276e8dfa6391", "openfda": {"nui": ["N0000180182"], "upc": ["0369292586013", "0369292582015", "0369292590010", "0369292584019", "0369292588017", "0369292580011", "0369292586105"], "unii": ["J6292F8L3D"], "rxcui": ["197754", "310670", "310671", "310672", "314034", "314035"], "spl_set_id": ["9a9e20dd-646a-4fe9-a345-1b5bda8e7775"], "pharm_class_epc": ["Typical Antipsychotic [EPC]"], "manufacturer_name": ["Amici Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (69292-582-01)", "package_ndc": "69292-582-01", "marketing_start_date": "20220418"}], "brand_name": "Haloperidol", "product_id": "69292-582_8c9cdd3d-9751-404a-9ceb-276e8dfa6391", "dosage_form": "TABLET", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "69292-582", "generic_name": "Haloperidol", "labeler_name": "Amici Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Haloperidol", "active_ingredients": [{"name": "HALOPERIDOL", "strength": "1 mg/1"}], "application_number": "ANDA071173", "marketing_category": "ANDA", "marketing_start_date": "20220418", "listing_expiration_date": "20261231"}