Package 25021-833-01

Brand: haloperidol decanoate

Generic: haloperidol decanoate
NDC Package

Package Facts

Identity

Package NDC 25021-833-01
Digits Only 2502183301
Product NDC 25021-833
Product ID 25021-833_62e2ca03-9545-4170-a750-d457aa2451a9
Description

10 VIAL in 1 CARTON (25021-833-01) / 1 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2017-11-15
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": "62e2ca03-9545-4170-a750-d457aa2451a9", "openfda": {"unii": ["AC20PJ4101"], "rxcui": ["859871", "1719803", "1719862"], "spl_set_id": ["b3167043-585f-482f-b8a7-591bc2721bd3"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (25021-833-01)  / 1 mL in 1 VIAL", "package_ndc": "25021-833-01", "marketing_start_date": "20171115"}], "brand_name": "haloperidol decanoate", "product_id": "25021-833_62e2ca03-9545-4170-a750-d457aa2451a9", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "25021-833", "generic_name": "haloperidol decanoate", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "haloperidol decanoate", "active_ingredients": [{"name": "HALOPERIDOL DECANOATE", "strength": "100 mg/mL"}], "application_number": "ANDA205241", "marketing_category": "ANDA", "marketing_start_date": "20171115", "listing_expiration_date": "20261231"}