Package 68001-579-48

Brand: haloperidol decanoate

Generic: haloperidol decanoate
NDC Package

Package Facts

Identity

Package NDC 68001-579-48
Digits Only 6800157948
Product NDC 68001-579
Description

5 AMPULE in 1 CARTON (68001-579-48) / 1 mL in 1 AMPULE (68001-579-59)

Marketing

Marketing Status
Marketed Since 2023-09-15
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": "048557ea-f859-f0f2-e063-6294a90af5ab", "openfda": {"upc": ["0368001578592", "0368001581417", "0368001579599", "0368001582414"], "unii": ["AC20PJ4101"], "rxcui": ["859871", "1719803", "1719862"], "spl_set_id": ["f2d14406-2ad4-4c5b-9c24-a026f27b415d"], "manufacturer_name": ["BluePoint Laboratories"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "5 AMPULE in 1 CARTON (68001-579-48)  / 1 mL in 1 AMPULE (68001-579-59)", "package_ndc": "68001-579-48", "marketing_start_date": "20230915"}], "brand_name": "HALOPERIDOL DECANOATE", "product_id": "68001-579_048557ea-f859-f0f2-e063-6294a90af5ab", "dosage_form": "INJECTION", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "68001-579", "generic_name": "HALOPERIDOL DECANOATE", "labeler_name": "BluePoint Laboratories", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HALOPERIDOL DECANOATE", "active_ingredients": [{"name": "HALOPERIDOL DECANOATE", "strength": "100 mg/mL"}], "application_number": "ANDA209101", "marketing_category": "ANDA", "marketing_start_date": "20230915", "listing_expiration_date": "20261231"}