Package 63323-471-41

Brand: haloperidol decanoate

Generic: haloperidol decanoate
NDC Package

Package Facts

Identity

Package NDC 63323-471-41
Digits Only 6332347141
Product NDC 63323-471
Product ID 63323-471_ffe1197b-99e4-4dee-922e-d1b528d84052
Description

1 VIAL in 1 CARTON (63323-471-41) / 1 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2000-07-12
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": "ffe1197b-99e4-4dee-922e-d1b528d84052", "openfda": {"unii": ["AC20PJ4101"], "rxcui": ["859871", "1719803"], "spl_set_id": ["262456c4-47e5-4713-8379-844f8f587495"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (63323-471-41)  / 1 mL in 1 VIAL", "package_ndc": "63323-471-41", "marketing_start_date": "20000712"}], "brand_name": "Haloperidol Decanoate", "product_id": "63323-471_ffe1197b-99e4-4dee-922e-d1b528d84052", "dosage_form": "INJECTION", "pharm_class": ["Typical Antipsychotic [EPC]"], "product_ndc": "63323-471", "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": "100 mg/mL"}], "application_number": "ANDA074893", "marketing_category": "ANDA", "marketing_start_date": "20000712", "listing_expiration_date": "20261231"}