Package 0904-7504-61

Brand: haloperidol

Generic: haloperidol
NDC Package

Package Facts

Identity

Package NDC 0904-7504-61
Digits Only 0904750461
Product NDC 0904-7504
Product ID 0904-7504_8a1014d0-d917-40b7-bddd-9ac97df91ef4
Description

100 BLISTER PACK in 1 CARTON (0904-7504-61) / 1 TABLET in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2025-01-28
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": "8a1014d0-d917-40b7-bddd-9ac97df91ef4", "openfda": {"nui": ["N0000180182"], "unii": ["J6292F8L3D"], "rxcui": ["314034"], "spl_set_id": ["8a1014d0-d917-40b7-bddd-9ac97df91ef4"], "pharm_class_epc": ["Typical Antipsychotic [EPC]"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-7504-61)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0904-7504-61", "marketing_start_date": "20250128"}], "brand_name": "Haloperidol", "product_id": "0904-7504_8a1014d0-d917-40b7-bddd-9ac97df91ef4", "dosage_form": "TABLET", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "0904-7504", "generic_name": "haloperidol", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Haloperidol", "active_ingredients": [{"name": "HALOPERIDOL", "strength": "2 mg/1"}], "application_number": "ANDA216918", "marketing_category": "ANDA", "marketing_start_date": "20250128", "listing_expiration_date": "20261231"}