Package 0904-7059-52

Brand: trospium chloride

Generic: trospium chloride
NDC Package

Package Facts

Identity

Package NDC 0904-7059-52
Digits Only 0904705952
Product NDC 0904-7059
Description

60 TABLET, FILM COATED in 1 BOTTLE (0904-7059-52)

Marketing

Marketing Status
Marketed Since 2015-11-16
Brand trospium chloride
Generic trospium chloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "239e206f-f6ca-4b35-a5b0-46d255cd57fa", "openfda": {"unii": ["1E6682427E"], "rxcui": ["857560"], "spl_set_id": ["35ae4d64-4625-4fdd-a2d4-e20b87c56876"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (0904-7059-52)", "package_ndc": "0904-7059-52", "marketing_start_date": "20151116"}], "brand_name": "Trospium Chloride", "product_id": "0904-7059_239e206f-f6ca-4b35-a5b0-46d255cd57fa", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "0904-7059", "generic_name": "Trospium Chloride", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trospium Chloride", "active_ingredients": [{"name": "TROSPIUM CHLORIDE", "strength": "20 mg/1"}], "application_number": "ANDA204945", "marketing_category": "ANDA", "marketing_start_date": "20151116", "listing_expiration_date": "20261231"}