Package 10135-725-01

Brand: fluphenazine hydrochloride

Generic: fluphenazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 10135-725-01
Digits Only 1013572501
Product NDC 10135-725
Product ID 10135-725_437e142c-e2e3-2b97-e063-6294a90a9266
Description

100 TABLET in 1 BOTTLE (10135-725-01)

Marketing

Marketing Status
Marketed Since 2021-06-01
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": "437e142c-e2e3-2b97-e063-6294a90a9266", "openfda": {"upc": ["0310135725014", "0310135726011"], "unii": ["ZOU145W1XL"], "rxcui": ["859841", "860918", "865117", "865123"], "spl_set_id": ["c69f07b1-660c-db03-e053-2995a90a5464"], "manufacturer_name": ["Marlex Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (10135-725-01)", "package_ndc": "10135-725-01", "marketing_start_date": "20210601"}], "brand_name": "FLUPHENAZINE HYDROCHLORIDE", "product_id": "10135-725_437e142c-e2e3-2b97-e063-6294a90a9266", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "10135-725", "generic_name": "FLUPHENAZINE HYDROCHLORIDE", "labeler_name": "Marlex Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "FLUPHENAZINE HYDROCHLORIDE", "active_ingredients": [{"name": "FLUPHENAZINE HYDROCHLORIDE", "strength": "1 mg/1"}], "application_number": "ANDA214674", "marketing_category": "ANDA", "marketing_start_date": "20210601", "listing_expiration_date": "20261231"}