Package 0069-0244-30

Brand: toviaz

Generic: fesoterodine fumarate
NDC Package

Package Facts

Identity

Package NDC 0069-0244-30
Digits Only 0069024430
Product NDC 0069-0244
Product ID 0069-0244_0e71efda-aa3d-4f4d-833f-c9e56bea3fff
Description

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0069-0244-30)

Marketing

Marketing Status
Marketed Since 2008-10-31
Brand toviaz
Generic fesoterodine fumarate
Sample Package No

Linked Drug Pages (1)

Toviaz ndc-match (0.95)

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 (0069-0244-30)", "package_ndc": "0069-0244-30", "marketing_start_date": "20081031"}], "brand_name": "Toviaz", "product_id": "0069-0244_0e71efda-aa3d-4f4d-833f-c9e56bea3fff", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "product_ndc": "0069-0244", "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": "8 mg/1"}], "application_number": "NDA022030", "marketing_category": "NDA", "marketing_start_date": "20081031", "listing_expiration_date": "20261231"}