Package 0404-9871-01
Brand: haloperidol lactate
Generic: haloperidolPackage Facts
Identity
Package NDC
0404-9871-01
Digits Only
0404987101
Product NDC
0404-9871
Description
1 VIAL in 1 BAG (0404-9871-01) / 1 mL in 1 VIAL
Marketing
Marketing Status
Brand
haloperidol lactate
Generic
haloperidol
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR"], "spl_id": "74d33642-a53d-4042-aa8f-87460d97fd9f", "openfda": {"unii": ["6387S86PK3"], "rxcui": ["1719646"], "spl_set_id": ["65df5d2d-79aa-41d4-866a-566e520320f7"], "manufacturer_name": ["Henry Schein, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BAG (0404-9871-01) / 1 mL in 1 VIAL", "package_ndc": "0404-9871-01", "marketing_start_date": "20220111"}], "brand_name": "Haloperidol Lactate", "product_id": "0404-9871_74d33642-a53d-4042-aa8f-87460d97fd9f", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "0404-9871", "generic_name": "Haloperidol", "labeler_name": "Henry Schein, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Haloperidol Lactate", "active_ingredients": [{"name": "HALOPERIDOL LACTATE", "strength": "5 mg/mL"}], "application_number": "ANDA078347", "marketing_category": "ANDA", "marketing_start_date": "20220111", "listing_expiration_date": "20271231"}