Package 51662-1524-1

Brand: haloperidol

Generic: haloperidol lactate
NDC Package

Package Facts

Identity

Package NDC 51662-1524-1
Digits Only 5166215241
Product NDC 51662-1524
Product ID 51662-1524_beb6d1cf-98dc-d0a5-e053-2995a90ace90
Description

1 mL in 1 VIAL (51662-1524-1)

Marketing

Marketing Status
Marketed Since 2021-03-29
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": "beb6d1cf-98dc-d0a5-e053-2995a90ace90", "openfda": {"unii": ["6387S86PK3"], "rxcui": ["1719646"], "spl_set_id": ["beb6d1cf-98db-d0a5-e053-2995a90ace90"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "1 mL in 1 VIAL (51662-1524-1)", "package_ndc": "51662-1524-1", "marketing_start_date": "20210329"}], "brand_name": "HALOPERIDOL", "product_id": "51662-1524_beb6d1cf-98dc-d0a5-e053-2995a90ace90", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "51662-1524", "generic_name": "Haloperidol Lactate", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HALOPERIDOL", "active_ingredients": [{"name": "HALOPERIDOL LACTATE", "strength": "5 mg/mL"}], "application_number": "ANDA075689", "marketing_category": "ANDA", "marketing_start_date": "20210329", "listing_expiration_date": "20261231"}