Package 54838-501-40

Brand: haloperidol

Generic: haloperidol
NDC Package

Package Facts

Identity

Package NDC 54838-501-40
Digits Only 5483850140
Product NDC 54838-501
Product ID 54838-501_898ee841-bdf7-4306-ac5c-282e522afd9f
Description

120 mL in 1 BOTTLE, DROPPER (54838-501-40)

Marketing

Marketing Status
Marketed Since 1993-09-28
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": "898ee841-bdf7-4306-ac5c-282e522afd9f", "openfda": {"upc": ["0354838501407"], "unii": ["6387S86PK3"], "rxcui": ["141935"], "spl_set_id": ["3e44fed0-6132-4881-a9cd-af6156c7af9c"], "manufacturer_name": ["Lannett Company, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "15 mL in 1 BOTTLE, DROPPER (54838-501-15)", "package_ndc": "54838-501-15", "marketing_start_date": "19930928"}, {"sample": false, "description": "120 mL in 1 BOTTLE, DROPPER (54838-501-40)", "package_ndc": "54838-501-40", "marketing_start_date": "19930928"}], "brand_name": "Haloperidol", "product_id": "54838-501_898ee841-bdf7-4306-ac5c-282e522afd9f", "dosage_form": "SOLUTION", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "54838-501", "generic_name": "Haloperidol", "labeler_name": "Lannett Company, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Haloperidol", "active_ingredients": [{"name": "HALOPERIDOL LACTATE", "strength": "2 mg/mL"}], "application_number": "ANDA073364", "marketing_category": "ANDA", "marketing_start_date": "19930928", "listing_expiration_date": "20261231"}