Package 68001-659-41

Brand: haloperidol decanoate

Generic: haloperidol decanoate
NDC Package

Package Facts

Identity

Package NDC 68001-659-41
Digits Only 6800165941
Product NDC 68001-659
Product ID 68001-659_49766ab0-8814-f685-e063-6394a90a303d
Description

1 VIAL, MULTI-DOSE in 1 CARTON (68001-659-41) / 5 mL in 1 VIAL, MULTI-DOSE

Marketing

Marketing Status
Marketed Since 2025-06-12
Brand haloperidol decanoate
Generic haloperidol decanoate
Sample Package No

Linked Drug Pages (1)

Haloperidol decanoate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR"], "spl_id": "49766ab0-8814-f685-e063-6394a90a303d", "openfda": {"unii": ["AC20PJ4101"], "rxcui": ["859871", "1719803", "1719862"], "spl_set_id": ["3d011250-a517-4c27-8ce3-d59d441ea61c"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 CARTON (68001-659-41)  / 5 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "68001-659-41", "marketing_start_date": "20250612"}], "brand_name": "Haloperidol decanoate", "product_id": "68001-659_49766ab0-8814-f685-e063-6394a90a303d", "dosage_form": "INJECTION", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "68001-659", "generic_name": "Haloperidol decanoate", "labeler_name": "BluePoint Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Haloperidol decanoate", "active_ingredients": [{"name": "HALOPERIDOL DECANOATE", "strength": "500 mg/5mL"}], "application_number": "ANDA211180", "marketing_category": "ANDA", "marketing_start_date": "20250612", "listing_expiration_date": "20271231"}