Package 25021-806-01

Brand: haloperidol

Generic: haloperidol lactate
NDC Package

Package Facts

Identity

Package NDC 25021-806-01
Digits Only 2502180601
Product NDC 25021-806
Product ID 25021-806_318a87c3-dab5-4137-af1e-afb0f7f4848b
Description

10 VIAL in 1 CARTON (25021-806-01) / 1 mL in 1 VIAL

Marketing

Marketing Status
Discontinued 2026-04-30
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": "318a87c3-dab5-4137-af1e-afb0f7f4848b", "openfda": {"unii": ["6387S86PK3"], "rxcui": ["1719646"], "spl_set_id": ["7ce7f23c-f58b-4b8b-a31a-47bd4e792345"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (25021-806-01)  / 1 mL in 1 VIAL", "package_ndc": "25021-806-01", "marketing_end_date": "20260430", "marketing_start_date": "20111024"}], "brand_name": "haloperidol", "product_id": "25021-806_318a87c3-dab5-4137-af1e-afb0f7f4848b", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "25021-806", "generic_name": "haloperidol lactate", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "haloperidol", "active_ingredients": [{"name": "HALOPERIDOL LACTATE", "strength": "5 mg/mL"}], "application_number": "ANDA091637", "marketing_category": "ANDA", "marketing_end_date": "20260430", "marketing_start_date": "20111024"}