Package 70518-4273-0

Brand: fluphenazine hydrochloride

Generic: fluphenazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 70518-4273-0
Digits Only 7051842730
Product NDC 70518-4273
Product ID 70518-4273_40191566-45bd-049b-e063-6394a90add51
Description

30 TABLET in 1 BLISTER PACK (70518-4273-0)

Marketing

Marketing Status
Marketed Since 2025-02-03
Brand fluphenazine hydrochloride
Generic fluphenazine hydrochloride
Sample Package No

Linked Drug Pages (0)

No linked drugs yet.

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "40191566-45bd-049b-e063-6394a90add51", "openfda": {"unii": ["ZOU145W1XL"], "rxcui": ["860918"], "spl_set_id": ["85720b55-3419-4e2c-95dd-22eec035d6f1"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-4273-0)", "package_ndc": "70518-4273-0", "marketing_start_date": "20250203"}], "brand_name": "Fluphenazine hydrochloride", "product_id": "70518-4273_40191566-45bd-049b-e063-6394a90add51", "dosage_form": "TABLET", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "70518-4273", "generic_name": "Fluphenazine hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluphenazine hydrochloride", "active_ingredients": [{"name": "FLUPHENAZINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA217410", "marketing_category": "ANDA", "marketing_start_date": "20250203", "listing_expiration_date": "20261231"}