Package 67046-1567-3

Brand: fluphenazine hydrochloride

Generic: fluphenazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 67046-1567-3
Digits Only 6704615673
Product NDC 67046-1567
Product ID 67046-1567_37c96bed-4f7d-8a59-e063-6294a90a3d58
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1567-3)

Marketing

Marketing Status
Marketed Since 2025-06-17
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": "37c96bed-4f7d-8a59-e063-6294a90a3d58", "openfda": {"unii": ["ZOU145W1XL"], "rxcui": ["865117"], "spl_set_id": ["37c9712b-95a1-fcc4-e063-6394a90aca50"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1567-3)", "package_ndc": "67046-1567-3", "marketing_start_date": "20250617"}], "brand_name": "Fluphenazine Hydrochloride", "product_id": "67046-1567_37c96bed-4f7d-8a59-e063-6294a90a3d58", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "67046-1567", "generic_name": "Fluphenazine Hydrochloride", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluphenazine Hydrochloride", "active_ingredients": [{"name": "FLUPHENAZINE HYDROCHLORIDE", "strength": "1 mg/1"}], "application_number": "ANDA218173", "marketing_category": "ANDA", "marketing_start_date": "20250617", "listing_expiration_date": "20261231"}