Fesoterodine Fumarate

FDA Approved: * January 4, 2023
Pharm Company: * AMERIGEN PHARMS LTD
Category: Urinary System

Fesoterodine (INN, used as the fumarate under the brand name Toviaz) is an antimuscarinic drug developed by Schwarz Pharma AG to treat overactive bladder syndrome (OAB).[2] It was approved by the European Medicines Agency in April 2007,[3] the US Food and Drug Administration on October 31, 2008 [4] and Health Canada on February 9, 2012.[5] Fesoterodine is a prodrug. It is broken down into its active metabolite, desfesoterodine, ... [wikipedia]

* May have multiple approval dates, manufacturers, or labelers.
1 Discussion

Dosage List

Fesoterodine Fumarate 4 mg Oral Tablet, Extended Release
NDC: 43598-247
Labeler:
Dr.reddy's Laboratories Inc.,
Fesoterodine Fumarate 8 mg Oral Tablet, Extended Release
NDC: 43598-248
Labeler:
Dr.reddy's Laboratories Inc.,
Fesoterodine Fumarate 4 mg Oral Tablet, Extended Release
NDC: 51407-661
Labeler:
Golden State Medical Supply, Inc.
Fesoterodine Fumarate 8 mg Oral Tablet, Extended Release
NDC: 51407-662
Labeler:
Golden State Medical Supply, Inc.
Fesoterodine Fumarate 4 mg Oral Tablet, Extended Release
NDC: 62332-175
Labeler:
Alembic Pharmaceuticals Inc.
Fesoterodine Fumarate 8 mg Oral Tablet, Extended Release
NDC: 62332-176
Labeler:
Alembic Pharmaceuticals Inc.
Fesoterodine Fumarate 8 mg Oral Tablet, Film Coated, Extended Release
NDC: 62559-376
Labeler:
Ani Pharmaceuticals, Inc.
Fesoterodine Fumarate 4 mg Oral Tablet, Extended Release
NDC: 65162-369
Labeler:
Amneal Pharmaceuticals LLC
Fesoterodine Fumarate 8 mg Oral Tablet, Extended Release
NDC: 65162-370
Labeler:
Amneal Pharmaceuticals LLC
Fesoterodine Fumarate 4 mg Oral Tablet, Film Coated, Extended Release
NDC: 65862-766
Labeler:
Aurobindo Pharma Limited

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