Package 72603-230-01

Brand: haloperidol decanoate

Generic: haloperidol decanoate
NDC Package

Package Facts

Identity

Package NDC 72603-230-01
Digits Only 7260323001
Product NDC 72603-230
Description

1 VIAL in 1 CARTON (72603-230-01) / 1 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2023-12-01
Brand haloperidol decanoate
Generic haloperidol decanoate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR"], "spl_id": "5f6d0f73-2b79-472a-94ce-ac8b0d31201d", "openfda": {"unii": ["AC20PJ4101"], "rxcui": ["1719803"], "spl_set_id": ["b83cb022-cfeb-4492-927b-0b461f7201d4"], "manufacturer_name": ["NorthStar RxLLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (72603-230-01)  / 1 mL in 1 VIAL", "package_ndc": "72603-230-01", "marketing_start_date": "20231201"}], "brand_name": "Haloperidol Decanoate", "product_id": "72603-230_5f6d0f73-2b79-472a-94ce-ac8b0d31201d", "dosage_form": "INJECTION", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "72603-230", "generic_name": "Haloperidol Decanoate", "labeler_name": "NorthStar RxLLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Haloperidol Decanoate", "active_ingredients": [{"name": "HALOPERIDOL DECANOATE", "strength": "100 mg/mL"}], "application_number": "ANDA216730", "marketing_category": "ANDA", "marketing_start_date": "20231201", "listing_expiration_date": "20261231"}