Package 67877-068-30
Brand: fesoterodine fumarate
Generic: fesoterodine fumaratePackage Facts
Identity
Package NDC
67877-068-30
Digits Only
6787706830
Product NDC
67877-068
Description
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (67877-068-30)
Marketing
Marketing Status
Brand
fesoterodine fumarate
Generic
fesoterodine fumarate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2fa76e78-8cb1-49ad-8f23-83ce759112be", "openfda": {"unii": ["EOS72165S7"], "rxcui": ["810071", "810077"], "spl_set_id": ["b1abd9cb-c480-437b-8531-e2de3e188363"], "manufacturer_name": ["Ascend Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (67877-068-30)", "package_ndc": "67877-068-30", "marketing_start_date": "20220609"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (67877-068-90)", "package_ndc": "67877-068-90", "marketing_start_date": "20220609"}], "brand_name": "Fesoterodine Fumarate", "product_id": "67877-068_2fa76e78-8cb1-49ad-8f23-83ce759112be", "dosage_form": "TABLET, EXTENDED RELEASE", "product_ndc": "67877-068", "generic_name": "Fesoterodine Fumarate", "labeler_name": "Ascend Laboratories, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Fesoterodine Fumarate", "active_ingredients": [{"name": "FESOTERODINE FUMARATE", "strength": "8 mg/1"}], "application_number": "ANDA204827", "marketing_category": "ANDA", "marketing_start_date": "20220609", "listing_expiration_date": "20261231"}