Package 63539-242-77

Brand: Toviaz

Generic: fesoterodine fumarate
NDC Package Sample

Package Facts

Identity

Package NDC 63539-242-77
Digits Only 6353924277
Product NDC 63539-242
Product ID 63539-242_a9f112ed-8afb-4c26-8de7-c0cdbfbc4375
Description

1 BLISTER PACK in 1 CARTON (63539-242-77) / 7 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2021-05-03
Brand Toviaz
Generic fesoterodine fumarate
Sample Package Yes

Linked Drug Pages (1)

Toviaz ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "a9f112ed-8afb-4c26-8de7-c0cdbfbc4375", "openfda": {"unii": ["EOS72165S7"], "rxcui": ["810071", "810075", "810077", "810079"], "spl_set_id": ["4f01dced-195a-4712-a614-d68012bc29df"], "manufacturer_name": ["U.S. Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": true, "description": "1 BLISTER PACK in 1 CARTON (63539-242-77)  / 7 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK", "package_ndc": "63539-242-77", "marketing_start_date": "20210503"}], "brand_name": "Toviaz", "product_id": "63539-242_a9f112ed-8afb-4c26-8de7-c0cdbfbc4375", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "product_ndc": "63539-242", "generic_name": "fesoterodine fumarate", "labeler_name": "U.S. Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Toviaz", "active_ingredients": [{"name": "FESOTERODINE FUMARATE", "strength": "4 mg/1"}], "application_number": "NDA022030", "marketing_category": "NDA", "marketing_start_date": "20081031", "listing_expiration_date": "20261231"}