Package 72205-069-91

Brand: haloperidol

Generic: haloperidol
NDC Package

Package Facts

Identity

Package NDC 72205-069-91
Digits Only 7220506991
Product NDC 72205-069
Product ID 72205-069_6d0f349d-2354-4358-8fa2-5e35da47eb00
Description

100 TABLET in 1 BOTTLE (72205-069-91)

Marketing

Marketing Status
Marketed Since 2022-11-22
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": "6d0f349d-2354-4358-8fa2-5e35da47eb00", "openfda": {"nui": ["N0000180182"], "upc": ["0372205067912", "0372205064911", "0372205065918", "0372205069916", "0372205065994", "0372205066991", "0372205068919", "0372205064997", "0372205067998", "0372205066915"], "unii": ["J6292F8L3D"], "rxcui": ["197754", "310670", "310671", "310672", "314034", "314035"], "spl_set_id": ["3a474e06-fb00-40cb-aa3a-6edad43c2c0a"], "pharm_class_epc": ["Typical Antipsychotic [EPC]"], "manufacturer_name": ["Novadoz Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72205-069-91)", "package_ndc": "72205-069-91", "marketing_start_date": "20221122"}], "brand_name": "HALOPERIDOL", "product_id": "72205-069_6d0f349d-2354-4358-8fa2-5e35da47eb00", "dosage_form": "TABLET", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "72205-069", "generic_name": "HALOPERIDOL", "labeler_name": "Novadoz Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HALOPERIDOL", "active_ingredients": [{"name": "HALOPERIDOL", "strength": "20 mg/1"}], "application_number": "ANDA216004", "marketing_category": "ANDA", "marketing_start_date": "20221118", "listing_expiration_date": "20271231"}