Package 0781-8046-01

Brand: perphenazine

Generic: perphenazine
NDC Package

Package Facts

Identity

Package NDC 0781-8046-01
Digits Only 0781804601
Product NDC 0781-8046
Description

100 TABLET, FILM COATED in 1 BOTTLE (0781-8046-01)

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": "9e348a80-ecb9-409b-91e7-3a48423314ff", "openfda": {"nui": ["N0000175746", "M0016525"], "unii": ["FTA7XXY4EZ"], "rxcui": ["198075", "198076", "198077", "198078"], "spl_set_id": ["fc32500c-cc42-4f85-9cee-88f983fcbc16"], "pharm_class_cs": ["Phenothiazines [CS]"], "pharm_class_epc": ["Phenothiazine [EPC]"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (0781-8046-01)", "package_ndc": "0781-8046-01", "marketing_end_date": "20270321", "marketing_start_date": "20180828"}], "brand_name": "Perphenazine", "product_id": "0781-8046_9e348a80-ecb9-409b-91e7-3a48423314ff", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "0781-8046", "generic_name": "Perphenazine", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Perphenazine", "active_ingredients": [{"name": "PERPHENAZINE", "strength": "2 mg/1"}], "application_number": "ANDA089685", "marketing_category": "ANDA", "marketing_end_date": "20270321", "marketing_start_date": "19881208"}