Package 0143-9502-01

Brand: haloperidol

Generic: haloperidol lactate
NDC Package

Package Facts

Identity

Package NDC 0143-9502-01
Digits Only 0143950201
Product NDC 0143-9502
Product ID 0143-9502_7b501c8b-902c-47ef-86e6-00c295473fd6
Description

1 VIAL in 1 BOX (0143-9502-01) / 10 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2001-06-19
Brand haloperidol
Generic haloperidol lactate
Sample Package No

Linked Drug Pages (1)

Haloperidol ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR"], "spl_id": "7b501c8b-902c-47ef-86e6-00c295473fd6", "openfda": {"unii": ["6387S86PK3"], "rxcui": ["204416", "1719646"], "spl_set_id": ["8397a841-f240-4767-9dcd-781e6d3f7c7f"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BOX (0143-9502-01)  / 10 mL in 1 VIAL", "package_ndc": "0143-9502-01", "marketing_start_date": "20010619"}], "brand_name": "Haloperidol", "product_id": "0143-9502_7b501c8b-902c-47ef-86e6-00c295473fd6", "dosage_form": "INJECTION", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "0143-9502", "generic_name": "Haloperidol Lactate", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Haloperidol", "active_ingredients": [{"name": "HALOPERIDOL LACTATE", "strength": "5 mg/mL"}], "application_number": "ANDA075858", "marketing_category": "ANDA", "marketing_start_date": "20010619", "listing_expiration_date": "20261231"}