Package 0904-7389-61

Brand: haloperidol

Generic: haloperidol
NDC Package

Package Facts

Identity

Package NDC 0904-7389-61
Digits Only 0904738961
Product NDC 0904-7389
Description

100 BLISTER PACK in 1 CARTON (0904-7389-61) / 1 TABLET in 1 BLISTER PACK

Marketing

Marketing Status
Discontinued 2026-06-30
Brand haloperidol
Generic haloperidol
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "5cdf5cc5-d403-44de-84bd-b94363e8bd60", "openfda": {"nui": ["N0000180182"], "unii": ["J6292F8L3D"], "rxcui": ["310670", "310671", "314034"], "spl_set_id": ["f5bfb3b9-0c6d-4f04-8bfc-d063cd8bb8ed"], "pharm_class_epc": ["Typical Antipsychotic [EPC]"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-7389-61)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "0904-7389-61", "marketing_end_date": "20260630", "marketing_start_date": "20230718"}], "brand_name": "Haloperidol", "product_id": "0904-7389_5cdf5cc5-d403-44de-84bd-b94363e8bd60", "dosage_form": "TABLET", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "0904-7389", "generic_name": "Haloperidol", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Haloperidol", "active_ingredients": [{"name": "HALOPERIDOL", "strength": ".5 mg/1"}], "application_number": "ANDA071173", "marketing_category": "ANDA", "marketing_end_date": "20260630", "marketing_start_date": "20230718"}