Package 72603-414-01

Brand: fesoterodine fumarate

Generic: fesoterodine fumarate
NDC Package

Package Facts

Identity

Package NDC 72603-414-01
Digits Only 7260341401
Product NDC 72603-414
Product ID 72603-414_2f97f9a3-4f2e-8409-e063-6394a90a7f94
Description

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72603-414-01)

Marketing

Marketing Status
Marketed Since 2024-05-01
Brand fesoterodine fumarate
Generic fesoterodine fumarate
Sample Package No

Linked Drug Pages (1)

FESOTERODINE FUMARATE ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2f97f9a3-4f2e-8409-e063-6394a90a7f94", "openfda": {"upc": ["0372603413014", "0372603414011"], "unii": ["EOS72165S7"], "rxcui": ["810071", "810077"], "spl_set_id": ["cb597206-1c75-4a4f-a17a-524a2010a4b9"], "manufacturer_name": ["NorthStar RxLLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72603-414-01)", "package_ndc": "72603-414-01", "marketing_start_date": "20240501"}], "brand_name": "FESOTERODINE FUMARATE", "product_id": "72603-414_2f97f9a3-4f2e-8409-e063-6394a90a7f94", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "product_ndc": "72603-414", "generic_name": "FESOTERODINE FUMARATE", "labeler_name": "NorthStar RxLLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "FESOTERODINE FUMARATE", "active_ingredients": [{"name": "FESOTERODINE FUMARATE", "strength": "8 mg/1"}], "application_number": "ANDA204792", "marketing_category": "ANDA", "marketing_start_date": "20240501", "listing_expiration_date": "20261231"}