Package 46708-789-31

Brand: fluphenazine hydrochloride

Generic: fluphenazine hydrochloride
NDC Package

Package Facts

Identity

Package NDC 46708-789-31
Digits Only 4670878931
Product NDC 46708-789
Product ID 46708-789_7c29fb1f-9403-4e55-abd9-36adfb152e8e
Description

100 TABLET, FILM COATED in 1 BOTTLE (46708-789-31)

Marketing

Marketing Status
Marketed Since 2024-07-25
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": "7c29fb1f-9403-4e55-abd9-36adfb152e8e", "openfda": {"upc": ["0346708788315", "0346708789312", "0346708791315", "0346708790318"], "unii": ["ZOU145W1XL"], "rxcui": ["859841", "860918", "865117", "865123"], "spl_set_id": ["7c29fb1f-9403-4e55-abd9-36adfb152e8e"], "manufacturer_name": ["Alembic Pharmaceuticals Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (46708-789-31)", "package_ndc": "46708-789-31", "marketing_start_date": "20240725"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (46708-789-71)", "package_ndc": "46708-789-71", "marketing_start_date": "20240725"}], "brand_name": "Fluphenazine Hydrochloride", "product_id": "46708-789_7c29fb1f-9403-4e55-abd9-36adfb152e8e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "46708-789", "generic_name": "Fluphenazine Hydrochloride", "labeler_name": "Alembic Pharmaceuticals Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fluphenazine Hydrochloride", "active_ingredients": [{"name": "FLUPHENAZINE HYDROCHLORIDE", "strength": "2.5 mg/1"}], "application_number": "ANDA218173", "marketing_category": "ANDA", "marketing_start_date": "20240725", "listing_expiration_date": "20261231"}