Package 90096-123-01

Brand: fluphenazine hydrochloride

Generic: fluphenazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 90096-123-01
Digits Only 9009612301
Product NDC 90096-123
Description

100 TABLET, FILM COATED in 1 BOTTLE (90096-123-01)

Marketing

Marketing Status
Marketed Since 2022-01-01
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": "bba99290-dad3-4e82-960e-bf274eb5e4b8", "openfda": {"upc": ["0390096123012"], "unii": ["ZOU145W1XL"], "rxcui": ["859841", "860918", "865117", "865123"], "spl_set_id": ["d9db3882-a7b5-435b-9d5a-a5e4ef7c2537"], "manufacturer_name": ["Zameer Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (90096-123-01)", "package_ndc": "90096-123-01", "marketing_start_date": "20220101"}], "brand_name": "Fluphenazine Hydrochloride", "product_id": "90096-123_bba99290-dad3-4e82-960e-bf274eb5e4b8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "90096-123", "generic_name": "Fluphenazine Hydrochloride", "labeler_name": "Zameer Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluphenazine Hydrochloride", "active_ingredients": [{"name": "FLUPHENAZINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA215141", "marketing_category": "ANDA", "marketing_start_date": "20220101", "listing_expiration_date": "20261231"}