Toviaz

Generic: fesoterodine fumarate

Labeler: U.S. Pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG NDA Active

Drug Facts

Product Profile

Brand Name Toviaz
Generic Name fesoterodine fumarate
Labeler U.S. Pharmaceuticals
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

FESOTERODINE FUMARATE 4 mg/1

Identifiers & Regulatory

Product NDC 63539-242
Product ID 63539-242_a9f112ed-8afb-4c26-8de7-c0cdbfbc4375
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA022030
Listing Expiration 2026-12-31
Marketing Start 2008-10-31

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 63539242
Hyphenated Format 63539-242

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name Toviaz (source: ndc)
Generic Name fesoterodine fumarate (source: ndc)
Application Number NDA022030 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 4 mg/1
source: ndc
Packaging
  • 1 BLISTER PACK in 1 CARTON (63539-242-77) / 7 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
source: ndc

Packages (1)

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

Ingredients (1)

FESOTERODINE FUMARATE (4 mg/1)

Linked Drug Pages (1)

Toviaz ndc-match (0.9)

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"}