Package 42023-129-01

Brand: fluphenazine decanoate

Generic: fluphenazine decanoate
NDC Package

Package Facts

Identity

Package NDC 42023-129-01
Digits Only 4202312901
Product NDC 42023-129
Product ID 42023-129_088a5d84-ec79-4e0e-96b1-29e31e6aa39f
Description

1 VIAL in 1 CARTON (42023-129-01) / 5 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2014-07-09
Brand fluphenazine decanoate
Generic fluphenazine decanoate
Sample Package No

Linked Drug Pages (1)

Fluphenazine Decanoate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "SUBCUTANEOUS"], "spl_id": "088a5d84-ec79-4e0e-96b1-29e31e6aa39f", "openfda": {"unii": ["FMU62K1L3C"], "rxcui": ["859824"], "spl_set_id": ["b580471f-44a1-4da0-96ad-2f537eabec3e"], "manufacturer_name": ["Endo USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (42023-129-01)  / 5 mL in 1 VIAL", "package_ndc": "42023-129-01", "marketing_start_date": "20140709"}], "brand_name": "Fluphenazine Decanoate", "product_id": "42023-129_088a5d84-ec79-4e0e-96b1-29e31e6aa39f", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "42023-129", "generic_name": "Fluphenazine Decanoate", "labeler_name": "Endo USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluphenazine Decanoate", "active_ingredients": [{"name": "FLUPHENAZINE DECANOATE", "strength": "25 mg/mL"}], "application_number": "ANDA203732", "marketing_category": "ANDA", "marketing_start_date": "20140709", "listing_expiration_date": "20261231"}