toviaz

Generic: fesoterodine fumarate

Labeler: pfizer laboratories div pfizer inc
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name toviaz
Generic Name fesoterodine fumarate
Labeler pfizer laboratories div pfizer inc
Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
Routes
ORAL
Active Ingredients

fesoterodine fumarate 4 mg/1

Manufacturer
Pfizer Laboratories Div Pfizer Inc

Identifiers & Regulatory

Product NDC 0069-0242
Product ID 0069-0242_0e71efda-aa3d-4f4d-833f-c9e56bea3fff
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 00690242
Hyphenated Format 0069-0242

Supplemental Identifiers

RxCUI
810071 810075 810077 810079
UPC
0300690242309 0300690244303
UNII
EOS72165S7

Packaging Origin

Original Packager
true

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
  • 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0069-0242-30)
source: ndc

Packages (1)

0069-0242-30 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0069-0242-30)

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": "0e71efda-aa3d-4f4d-833f-c9e56bea3fff", "openfda": {"upc": ["0300690242309", "0300690244303"], "unii": ["EOS72165S7"], "rxcui": ["810071", "810075", "810077", "810079"], "spl_set_id": ["5be745f0-8ae7-4c3c-9962-37d6263326f1"], "manufacturer_name": ["Pfizer Laboratories Div Pfizer Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0069-0242-30)", "package_ndc": "0069-0242-30", "marketing_start_date": "20081031"}], "brand_name": "Toviaz", "product_id": "0069-0242_0e71efda-aa3d-4f4d-833f-c9e56bea3fff", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "product_ndc": "0069-0242", "generic_name": "fesoterodine fumarate", "labeler_name": "Pfizer Laboratories Div Pfizer Inc", "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"}