Package 65162-369-09

Brand: fesoterodine fumarate

Generic: fesoterodine fumarate
NDC Package

Package Facts

Identity

Package NDC 65162-369-09
Digits Only 6516236909
Product NDC 65162-369
Description

90 TABLET, EXTENDED RELEASE in 1 BOTTLE (65162-369-09)

Marketing

Marketing Status
Marketed Since 2023-01-06
Brand fesoterodine fumarate
Generic fesoterodine fumarate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "84a0cad7-6b3b-46f3-8797-c0b922026154", "openfda": {"upc": ["0365162370034", "0365162369038"], "unii": ["EOS72165S7"], "rxcui": ["810071", "810077"], "spl_set_id": ["1d3fdfcf-7406-4be0-90e9-b10c9257bf69"], "manufacturer_name": ["Amneal Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (65162-369-03)", "package_ndc": "65162-369-03", "marketing_start_date": "20230106"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (65162-369-09)", "package_ndc": "65162-369-09", "marketing_start_date": "20230106"}], "brand_name": "Fesoterodine Fumarate", "product_id": "65162-369_84a0cad7-6b3b-46f3-8797-c0b922026154", "dosage_form": "TABLET, EXTENDED RELEASE", "product_ndc": "65162-369", "generic_name": "Fesoterodine Fumarate", "labeler_name": "Amneal Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fesoterodine Fumarate", "active_ingredients": [{"name": "FESOTERODINE FUMARATE", "strength": "4 mg/1"}], "application_number": "ANDA205002", "marketing_category": "ANDA", "marketing_start_date": "20230106", "listing_expiration_date": "20261231"}