Package 70710-1488-1

Brand: fluphenazine hydrochloride

Generic: fluphenazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70710-1488-1
Digits Only 7071014881
Product NDC 70710-1488
Description

100 TABLET, FILM COATED in 1 BOTTLE (70710-1488-1)

Marketing

Marketing Status
Marketed Since 2021-05-28
Brand fluphenazine hydrochloride
Generic fluphenazine hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "130b45fa-6dbd-46cc-a937-ab8ef1ec0718", "openfda": {"unii": ["ZOU145W1XL"], "rxcui": ["859841", "860918", "865117", "865123"], "spl_set_id": ["c4448579-3ccb-442e-8950-a219d1f01a98"], "manufacturer_name": ["Zydus Pharmaceuticals (USA) Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (70710-1488-1)", "package_ndc": "70710-1488-1", "marketing_start_date": "20210528"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (70710-1488-5)", "package_ndc": "70710-1488-5", "marketing_start_date": "20210528"}], "brand_name": "Fluphenazine Hydrochloride", "product_id": "70710-1488_130b45fa-6dbd-46cc-a937-ab8ef1ec0718", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "70710-1488", "generic_name": "Fluphenazine Hydrochloride", "labeler_name": "Zydus Pharmaceuticals (USA) Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluphenazine Hydrochloride", "active_ingredients": [{"name": "FLUPHENAZINE HYDROCHLORIDE", "strength": "1 mg/1"}], "application_number": "ANDA214552", "marketing_category": "ANDA", "marketing_start_date": "20210528", "listing_expiration_date": "20261231"}