Package 31722-034-30

Brand: fesoterodine fumarate

Generic: fesoterodine fumarate
NDC Package

Package Facts

Identity

Package NDC 31722-034-30
Digits Only 3172203430
Product NDC 31722-034
Product ID 31722-034_2f836bf8-7034-db2e-e063-6394a90a3a3e
Description

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (31722-034-30)

Marketing

Marketing Status
Marketed Since 2024-01-09
Brand fesoterodine fumarate
Generic fesoterodine fumarate
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2f836bf8-7034-db2e-e063-6394a90a3a3e", "openfda": {"upc": ["0331722033305", "0331722034302"], "unii": ["EOS72165S7"], "rxcui": ["810071", "810077"], "spl_set_id": ["dc532c6c-ff0d-488a-8a92-b1b0f37c944e"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (31722-034-30)", "package_ndc": "31722-034-30", "marketing_start_date": "20240109"}, {"sample": false, "description": "90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (31722-034-90)", "package_ndc": "31722-034-90", "marketing_start_date": "20240109"}], "brand_name": "FESOTERODINE FUMARATE", "product_id": "31722-034_2f836bf8-7034-db2e-e063-6394a90a3a3e", "dosage_form": "TABLET, FILM COATED, EXTENDED RELEASE", "product_ndc": "31722-034", "generic_name": "FESOTERODINE FUMARATE", "labeler_name": "Camber Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "FESOTERODINE FUMARATE", "active_ingredients": [{"name": "FESOTERODINE FUMARATE", "strength": "8 mg/1"}], "application_number": "ANDA204792", "marketing_category": "ANDA", "marketing_start_date": "20240109", "listing_expiration_date": "20261231"}