Package 0378-0214-10

Brand: haloperidol

Generic: haloperidol
NDC Package

Package Facts

Identity

Package NDC 0378-0214-10
Digits Only 0378021410
Product NDC 0378-0214
Product ID 0378-0214_1b33ae94-4fa5-4298-a713-3e049c47588c
Description

1000 TABLET in 1 BOTTLE, PLASTIC (0378-0214-10)

Marketing

Marketing Status
Discontinued 2027-02-28
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": "1b33ae94-4fa5-4298-a713-3e049c47588c", "openfda": {"nui": ["N0000180182"], "upc": ["0303780351011"], "unii": ["J6292F8L3D"], "rxcui": ["197754", "310670", "310671", "310672", "314034", "314035"], "spl_set_id": ["c559b0b0-4087-d12a-e718-c18ccb6811e6"], "pharm_class_epc": ["Typical Antipsychotic [EPC]"], "manufacturer_name": ["Mylan Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (0378-0214-10)", "package_ndc": "0378-0214-10", "marketing_end_date": "20270228", "marketing_start_date": "19860610"}], "brand_name": "Haloperidol", "product_id": "0378-0214_1b33ae94-4fa5-4298-a713-3e049c47588c", "dosage_form": "TABLET", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "0378-0214", "generic_name": "haloperidol", "labeler_name": "Mylan Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Haloperidol", "active_ingredients": [{"name": "HALOPERIDOL", "strength": "2 mg/1"}], "application_number": "ANDA070278", "marketing_category": "ANDA", "marketing_end_date": "20270228", "marketing_start_date": "19860610"}