Package 0143-9295-01

Brand: haloperidol decanoate

Generic: haloperidol decanoate
NDC Package

Package Facts

Identity

Package NDC 0143-9295-01
Digits Only 0143929501
Product NDC 0143-9295
Description

1 VIAL in 1 BOX (0143-9295-01) / 1 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 1998-10-01
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": "4d57ff6f-2f61-49f5-95d7-cbfa3505f020", "openfda": {"unii": ["AC20PJ4101"], "rxcui": ["859871", "1719803"], "spl_set_id": ["914026da-103a-4466-abd5-3763e9d55b67"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BOX (0143-9295-01)  / 1 mL in 1 VIAL", "package_ndc": "0143-9295-01", "marketing_start_date": "19981001"}], "brand_name": "Haloperidol Decanoate", "product_id": "0143-9295_4d57ff6f-2f61-49f5-95d7-cbfa3505f020", "dosage_form": "INJECTION", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "0143-9295", "generic_name": "Haloperidol Decanoate", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Haloperidol Decanoate", "active_ingredients": [{"name": "HALOPERIDOL DECANOATE", "strength": "100 mg/mL"}], "application_number": "ANDA075305", "marketing_category": "ANDA", "marketing_start_date": "19981001", "listing_expiration_date": "20261231"}