Package 0615-8355-39

Brand: haloperidol

Generic: haloperidol
NDC Package

Package Facts

Identity

Package NDC 0615-8355-39
Digits Only 0615835539
Product NDC 0615-8355
Product ID 0615-8355_b2861983-5663-4c40-b300-4a5248c6c892
Description

30 TABLET in 1 BLISTER PACK (0615-8355-39)

Marketing

Marketing Status
Discontinued 2026-05-31
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": "b2861983-5663-4c40-b300-4a5248c6c892", "openfda": {"nui": ["N0000180182"], "unii": ["J6292F8L3D"], "rxcui": ["310672", "314035"], "spl_set_id": ["e7dcb764-d58d-4476-b981-3bd54f0d896e"], "pharm_class_epc": ["Typical Antipsychotic [EPC]"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (0615-8355-39)", "package_ndc": "0615-8355-39", "marketing_end_date": "20260531", "marketing_start_date": "20201020"}], "brand_name": "Haloperidol", "product_id": "0615-8355_b2861983-5663-4c40-b300-4a5248c6c892", "dosage_form": "TABLET", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "0615-8355", "generic_name": "Haloperidol", "labeler_name": "NCS HealthCare of KY, LLC dba Vangard Labs", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Haloperidol", "active_ingredients": [{"name": "HALOPERIDOL", "strength": "5 mg/1"}], "application_number": "ANDA211061", "marketing_category": "ANDA", "marketing_end_date": "20260531", "marketing_start_date": "20200109"}