Package 50742-193-90

Brand: tolcapone

Generic: tolcapone
NDC Package

Package Facts

Identity

Package NDC 50742-193-90
Digits Only 5074219390
Product NDC 50742-193
Description

90 TABLET in 1 BOTTLE (50742-193-90)

Marketing

Marketing Status
Marketed Since 2018-08-21
Brand tolcapone
Generic tolcapone
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "b0eeccbf-775d-4ff7-805c-cc176f965198", "openfda": {"nui": ["N0000175756", "N0000175757"], "unii": ["CIF6334OLY"], "rxcui": ["200220"], "spl_set_id": ["d94891be-2fef-4e39-8e35-ab7afe93e78e"], "pharm_class_epc": ["Catechol-O-Methyltransferase Inhibitor [EPC]"], "pharm_class_moa": ["Catechol O-Methyltransferase Inhibitors [MoA]"], "manufacturer_name": ["Ingenus Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (50742-193-90)", "package_ndc": "50742-193-90", "marketing_start_date": "20180821"}], "brand_name": "TOLCAPONE", "product_id": "50742-193_b0eeccbf-775d-4ff7-805c-cc176f965198", "dosage_form": "TABLET", "pharm_class": ["Catechol O-Methyltransferase Inhibitors [MoA]", "Catechol-O-Methyltransferase Inhibitor [EPC]"], "product_ndc": "50742-193", "generic_name": "tolcapone", "labeler_name": "Ingenus Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "TOLCAPONE", "active_ingredients": [{"name": "TOLCAPONE", "strength": "100 mg/1"}], "application_number": "ANDA208937", "marketing_category": "ANDA", "marketing_start_date": "20180821", "listing_expiration_date": "20261231"}