Package 70069-866-10

Brand: haloperidol decanoate

Generic: haloperidol decanoate
NDC Package

Package Facts

Identity

Package NDC 70069-866-10
Digits Only 7006986610
Product NDC 70069-866
Product ID 70069-866_75154f5d-21e4-4278-85f9-78a4a4e85741
Description

10 VIAL in 1 CARTON (70069-866-10) / 1 mL in 1 VIAL (70069-866-01)

Marketing

Marketing Status
Marketed Since 2025-09-29
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": "75154f5d-21e4-4278-85f9-78a4a4e85741", "openfda": {"upc": ["0370069868010", "0370069867013"], "unii": ["AC20PJ4101"], "rxcui": ["859871", "1719803", "1719862"], "spl_set_id": ["068fc913-779d-44c6-9585-3aa80e751bee"], "manufacturer_name": ["Somerset Therapeutics, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (70069-866-10)  / 1 mL in 1 VIAL (70069-866-01)", "package_ndc": "70069-866-10", "marketing_start_date": "20250929"}], "brand_name": "HALOPERIDOL DECANOATE", "product_id": "70069-866_75154f5d-21e4-4278-85f9-78a4a4e85741", "dosage_form": "INJECTION", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "70069-866", "generic_name": "HALOPERIDOL DECANOATE", "labeler_name": "Somerset Therapeutics, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HALOPERIDOL DECANOATE", "active_ingredients": [{"name": "HALOPERIDOL DECANOATE", "strength": "50 mg/mL"}], "application_number": "ANDA219168", "marketing_category": "ANDA", "marketing_start_date": "20250929", "listing_expiration_date": "20261231"}