Package 59651-688-05

Brand: fluphenazine hydrochloride

Generic: fluphenazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 59651-688-05
Digits Only 5965168805
Product NDC 59651-688
Product ID 59651-688_1109b107-f7af-45b7-b8ee-709c59123074
Description

500 TABLET in 1 BOTTLE (59651-688-05)

Marketing

Marketing Status
Marketed Since 2023-08-18
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": ["ORAL"], "spl_id": "1109b107-f7af-45b7-b8ee-709c59123074", "openfda": {"unii": ["ZOU145W1XL"], "rxcui": ["859841", "860918", "865117", "865123"], "spl_set_id": ["e73764e7-e666-4ad3-a029-04a528dc1c9e"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (59651-688-01)", "package_ndc": "59651-688-01", "marketing_start_date": "20230818"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (59651-688-05)", "package_ndc": "59651-688-05", "marketing_start_date": "20230818"}], "brand_name": "Fluphenazine Hydrochloride", "product_id": "59651-688_1109b107-f7af-45b7-b8ee-709c59123074", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "59651-688", "generic_name": "Fluphenazine Hydrochloride", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluphenazine Hydrochloride", "active_ingredients": [{"name": "FLUPHENAZINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA218055", "marketing_category": "ANDA", "marketing_start_date": "20230818", "listing_expiration_date": "20261231"}