Package 67046-1603-3

Brand: haloperidol

Generic: haloperidol
NDC Package

Package Facts

Identity

Package NDC 67046-1603-3
Digits Only 6704616033
Product NDC 67046-1603
Product ID 67046-1603_40187e11-e94a-e759-e063-6394a90a4840
Description

30 TABLET in 1 BLISTER PACK (67046-1603-3)

Marketing

Marketing Status
Marketed Since 2025-10-01
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": "40187e11-e94a-e759-e063-6394a90a4840", "openfda": {"nui": ["N0000180182"], "unii": ["J6292F8L3D"], "rxcui": ["310672"], "spl_set_id": ["40187e83-1144-db0e-e063-6394a90a42df"], "pharm_class_epc": ["Typical Antipsychotic [EPC]"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (67046-1603-3)", "package_ndc": "67046-1603-3", "marketing_start_date": "20251001"}], "brand_name": "Haloperidol", "product_id": "67046-1603_40187e11-e94a-e759-e063-6394a90a4840", "dosage_form": "TABLET", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "67046-1603", "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": "ANDA218789", "marketing_category": "ANDA", "marketing_start_date": "20251001", "listing_expiration_date": "20261231"}