Package 63323-281-10

Brand: fluphenazine hydrochloride

Generic: fluphenazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63323-281-10
Digits Only 6332328110
Product NDC 63323-281
Product ID 63323-281_cefdb059-d32b-44f2-8dd6-fd2a29b3ba70
Description

1 VIAL in 1 BOX (63323-281-10) / 10 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2010-12-28
Brand fluphenazine hydrochloride
Generic fluphenazine hydrochloride
Sample Package No

Linked Drug Pages (1)

Fluphenazine Hydrochloride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR"], "spl_id": "cefdb059-d32b-44f2-8dd6-fd2a29b3ba70", "openfda": {"unii": ["ZOU145W1XL"], "rxcui": ["865129"], "spl_set_id": ["d571f04f-6190-42f2-932c-5a075fd978b9"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BOX (63323-281-10)  / 10 mL in 1 VIAL", "package_ndc": "63323-281-10", "marketing_start_date": "20101228"}], "brand_name": "Fluphenazine Hydrochloride", "product_id": "63323-281_cefdb059-d32b-44f2-8dd6-fd2a29b3ba70", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "63323-281", "generic_name": "FLUPHENAZINE HYDROCHLORIDE", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluphenazine Hydrochloride", "active_ingredients": [{"name": "FLUPHENAZINE HYDROCHLORIDE", "strength": "2.5 mg/mL"}], "application_number": "ANDA089556", "marketing_category": "ANDA", "marketing_start_date": "20101228", "listing_expiration_date": "20261231"}