Package 63323-469-01

Brand: haloperidol decanoate

Generic: haloperidol decanoate
NDC Package

Package Facts

Identity

Package NDC 63323-469-01
Digits Only 6332346901
Product NDC 63323-469
Description

1 VIAL in 1 CARTON (63323-469-01) / 1 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2000-02-16
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": "86dff2aa-2ab3-42fc-989e-619b13ace573", "openfda": {"unii": ["AC20PJ4101"], "rxcui": ["859867", "859871", "1719803", "1719862"], "spl_set_id": ["ca9896e0-fb2e-46a4-8700-20d144c14764"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (63323-469-01)  / 1 mL in 1 VIAL", "package_ndc": "63323-469-01", "marketing_start_date": "20000216"}, {"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 CARTON (63323-469-05)  / 5 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "63323-469-05", "marketing_start_date": "20000216"}], "brand_name": "Haloperidol Decanoate", "product_id": "63323-469_86dff2aa-2ab3-42fc-989e-619b13ace573", "dosage_form": "INJECTION", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "63323-469", "generic_name": "HALOPERIDOL DECANOATE", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Haloperidol Decanoate", "active_ingredients": [{"name": "HALOPERIDOL DECANOATE", "strength": "50 mg/mL"}], "application_number": "ANDA074893", "marketing_category": "ANDA", "marketing_start_date": "20000216", "listing_expiration_date": "20261231"}