Package 70518-1109-0

Brand: perphenazine

Generic: perphenazine
NDC Package

Package Facts

Identity

Package NDC 70518-1109-0
Digits Only 7051811090
Product NDC 70518-1109
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1109-0)

Marketing

Marketing Status
Marketed Since 2018-04-11
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": "485a1434-53e1-abcf-e063-6294a90a9a74", "openfda": {"nui": ["N0000175746", "M0016525"], "unii": ["FTA7XXY4EZ"], "rxcui": ["198075"], "spl_set_id": ["cf41a02d-c881-4b40-b99c-d5b79dbd645b"], "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 (70518-1109-0)", "package_ndc": "70518-1109-0", "marketing_start_date": "20180411"}], "brand_name": "Perphenazine", "product_id": "70518-1109_485a1434-53e1-abcf-e063-6294a90a9a74", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Phenothiazine [EPC]", "Phenothiazines [CS]"], "product_ndc": "70518-1109", "generic_name": "Perphenazine", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Perphenazine", "active_ingredients": [{"name": "PERPHENAZINE", "strength": "16 mg/1"}], "application_number": "ANDA205973", "marketing_category": "ANDA", "marketing_start_date": "20180411", "listing_expiration_date": "20271231"}