Package 65862-766-30

Brand: fesoterodine fumarate

Generic: fesoterodine fumarate
NDC Package

Package Facts

Identity

Package NDC 65862-766-30
Digits Only 6586276630
Product NDC 65862-766
Product ID 65862-766_33d91059-f2d5-482f-a47f-b1dccb7c5b22
Description

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-766-30)

Marketing

Marketing Status
Marketed Since 2022-06-17
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": "33d91059-f2d5-482f-a47f-b1dccb7c5b22", "openfda": {"upc": ["0365862766304", "0365862767301"], "unii": ["EOS72165S7"], "rxcui": ["810071", "810077"], "spl_set_id": ["dc8f6158-3c2b-4ec0-a951-e04468b83bb1"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-766-30)", "package_ndc": "65862-766-30", "marketing_start_date": "20220617"}], "brand_name": "FESOTERODINE FUMARATE", "product_id": "65862-766_33d91059-f2d5-482f-a47f-b1dccb7c5b22", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "product_ndc": "65862-766", "generic_name": "FESOTERODINE FUMARATE", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "FESOTERODINE FUMARATE", "active_ingredients": [{"name": "FESOTERODINE FUMARATE", "strength": "4 mg/1"}], "application_number": "ANDA205007", "marketing_category": "ANDA", "marketing_start_date": "20220617", "listing_expiration_date": "20261231"}