Package 16571-892-50

Brand: fluphenazine hydrochoride

Generic: fluphenazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 16571-892-50
Digits Only 1657189250
Product NDC 16571-892
Product ID 16571-892_5e7076f6-426b-45c2-865f-7be79fe81205
Description

500 TABLET, FILM COATED in 1 CONTAINER (16571-892-50)

Marketing

Marketing Status
Marketed Since 2024-06-07
Brand fluphenazine hydrochoride
Generic fluphenazine hydrochloride
Sample Package No

Linked Drug Pages (1)

Fluphenazine Hydrochoride ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "5e7076f6-426b-45c2-865f-7be79fe81205", "openfda": {"unii": ["ZOU145W1XL"], "rxcui": ["859841", "860918", "865117", "865123"], "spl_set_id": ["9fd44ab9-79bb-472e-8434-c3d786b42de5"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 CONTAINER (16571-892-09)", "package_ndc": "16571-892-09", "marketing_start_date": "20240607"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 CONTAINER (16571-892-50)", "package_ndc": "16571-892-50", "marketing_start_date": "20240607"}], "brand_name": "Fluphenazine Hydrochoride", "product_id": "16571-892_5e7076f6-426b-45c2-865f-7be79fe81205", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "16571-892", "generic_name": "fluphenazine hydrochloride", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluphenazine Hydrochoride", "active_ingredients": [{"name": "FLUPHENAZINE HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA218283", "marketing_category": "ANDA", "marketing_start_date": "20240607", "listing_expiration_date": "20261231"}