Package 67046-0053-3

Brand: haloperidol

Generic: haloperidol
NDC Package

Package Facts

Identity

Package NDC 67046-0053-3
Digits Only 6704600533
Product NDC 67046-0053
Product ID 67046-0053_38f58246-c2e2-01f8-e063-6394a90a3b7d
Description

30 TABLET in 1 BLISTER PACK (67046-0053-3)

Marketing

Marketing Status
Marketed Since 2025-07-02
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": "38f58246-c2e2-01f8-e063-6394a90a3b7d", "openfda": {"nui": ["N0000180182"], "unii": ["J6292F8L3D"], "rxcui": ["310672"], "spl_set_id": ["38f59751-4741-f588-e063-6294a90a6528"], "pharm_class_epc": ["Typical Antipsychotic [EPC]"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (67046-0053-3)", "package_ndc": "67046-0053-3", "marketing_start_date": "20250702"}], "brand_name": "Haloperidol", "product_id": "67046-0053_38f58246-c2e2-01f8-e063-6394a90a3b7d", "dosage_form": "TABLET", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "67046-0053", "generic_name": "Haloperidol", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Haloperidol", "active_ingredients": [{"name": "HALOPERIDOL", "strength": "5 mg/1"}], "application_number": "ANDA071173", "marketing_category": "ANDA", "marketing_start_date": "20250702", "listing_expiration_date": "20261231"}