Package 31722-386-05

Brand: fluphenazine hydrochloride

Generic: fluphenazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 31722-386-05
Digits Only 3172238605
Product NDC 31722-386
Product ID 31722-386_4468c081-e6a4-bbbf-e063-6294a90aa886
Description

500 TABLET, FILM COATED in 1 BOTTLE (31722-386-05)

Marketing

Marketing Status
Marketed Since 2025-11-18
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": "4468c081-e6a4-bbbf-e063-6294a90aa886", "openfda": {"upc": ["0331722386012", "0331722387019", "0331722385015"], "unii": ["ZOU145W1XL"], "rxcui": ["859841", "860918", "865117", "865123"], "spl_set_id": ["4dd61338-8e4b-41c6-99d8-811a8e990c4e"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (31722-386-01)", "package_ndc": "31722-386-01", "marketing_start_date": "20251118"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (31722-386-05)", "package_ndc": "31722-386-05", "marketing_start_date": "20251118"}], "brand_name": "Fluphenazine Hydrochloride", "product_id": "31722-386_4468c081-e6a4-bbbf-e063-6294a90aa886", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "31722-386", "generic_name": "Fluphenazine Hydrochloride", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluphenazine Hydrochloride", "active_ingredients": [{"name": "FLUPHENAZINE HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA218769", "marketing_category": "ANDA", "marketing_start_date": "20251118", "listing_expiration_date": "20261231"}