Package 67046-1547-3

Brand: fluphenazine hydrochloride

Generic: fluphenazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67046-1547-3
Digits Only 6704615473
Product NDC 67046-1547
Product ID 67046-1547_325c8a4a-a623-015f-e063-6294a90a92e3
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1547-3)

Marketing

Marketing Status
Marketed Since 2025-04-09
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": "325c8a4a-a623-015f-e063-6294a90a92e3", "openfda": {"unii": ["ZOU145W1XL"], "rxcui": ["860918"], "spl_set_id": ["325c8c34-2858-af36-e063-6394a90a7814"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1547-3)", "package_ndc": "67046-1547-3", "marketing_start_date": "20250409"}], "brand_name": "Fluphenazine Hydrochloride", "product_id": "67046-1547_325c8a4a-a623-015f-e063-6294a90a92e3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "67046-1547", "generic_name": "Fluphenazine Hydrochloride", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluphenazine Hydrochloride", "active_ingredients": [{"name": "FLUPHENAZINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA218173", "marketing_category": "ANDA", "marketing_start_date": "20250409", "listing_expiration_date": "20261231"}