Package 0143-9319-25
Brand: haloperidol
Generic: haloperidol lactatePackage Facts
Identity
Package NDC
0143-9319-25
Digits Only
0143931925
Product NDC
0143-9319
Description
25 VIAL in 1 BOX (0143-9319-25) / 1 mL in 1 VIAL
Marketing
Marketing Status
Brand
haloperidol
Generic
haloperidol lactate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR"], "spl_id": "b93ee0dc-a484-402b-8345-3d68ba0c689a", "openfda": {"unii": ["6387S86PK3"], "rxcui": ["1719646"], "spl_set_id": ["ec7a3560-71c3-43f5-bc6c-d51eadfd2aa1"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 BOX (0143-9319-25) / 1 mL in 1 VIAL", "package_ndc": "0143-9319-25", "marketing_start_date": "20180914"}], "brand_name": "Haloperidol", "product_id": "0143-9319_b93ee0dc-a484-402b-8345-3d68ba0c689a", "dosage_form": "INJECTION", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "0143-9319", "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": "20180914", "listing_expiration_date": "20261231"}