Package 70954-276-20

Brand: fluphenazine hydrochloride

Generic: fluphenazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70954-276-20
Digits Only 7095427620
Product NDC 70954-276
Product ID 70954-276_b62e66ce-9c80-46f1-bb86-68f7f73c487c
Description

500 TABLET in 1 BOTTLE (70954-276-20)

Marketing

Marketing Status
Marketed Since 2021-03-01
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": "b62e66ce-9c80-46f1-bb86-68f7f73c487c", "openfda": {"upc": ["0370954275107", "0370954276104", "0370954276203", "0370954275206", "0370954273103"], "unii": ["ZOU145W1XL"], "rxcui": ["859841", "860918", "865117", "865123"], "spl_set_id": ["6218cbd2-1f7f-40fa-92d2-5d5b0d7fa60b"], "manufacturer_name": ["ANI Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (70954-276-10)", "package_ndc": "70954-276-10", "marketing_start_date": "20210301"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (70954-276-20)", "package_ndc": "70954-276-20", "marketing_start_date": "20210301"}], "brand_name": "Fluphenazine Hydrochloride", "product_id": "70954-276_b62e66ce-9c80-46f1-bb86-68f7f73c487c", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "70954-276", "generic_name": "Fluphenazine Hydrochloride", "labeler_name": "ANI Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluphenazine Hydrochloride", "active_ingredients": [{"name": "FLUPHENAZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA214674", "marketing_category": "ANDA", "marketing_start_date": "20210301", "listing_expiration_date": "20261231"}