Package 70518-4112-0

Brand: Perphenazine

Generic: Perphenazine
NDC Package

Package Facts

Identity

Package NDC 70518-4112-0
Digits Only 7051841120
Product NDC 70518-4112
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4112-0)

Marketing

Marketing Status
Discontinued 2027-03-21
Brand Perphenazine
Generic Perphenazine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1bcdd8e4-c483-22ca-e063-6294a90af66a", "openfda": {"nui": ["N0000175746", "M0016525"], "unii": ["FTA7XXY4EZ"], "rxcui": ["198077"], "spl_set_id": ["9588d223-41e4-4bb2-9306-f082498404c5"], "pharm_class_cs": ["Phenothiazines [CS]"], "pharm_class_epc": ["Phenothiazine [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4112-0)", "package_ndc": "70518-4112-0", "marketing_end_date": "20270321", "marketing_start_date": "20240625"}], "brand_name": "Perphenazine", "product_id": "70518-4112_1bcdd8e4-c483-22ca-e063-6294a90af66a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "70518-4112", "generic_name": "Perphenazine", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Perphenazine", "active_ingredients": [{"name": "PERPHENAZINE", "strength": "4 mg/1"}], "application_number": "ANDA089685", "marketing_category": "ANDA", "marketing_end_date": "20270321", "marketing_start_date": "20240625"}