United States · FDA National Drug Code directory
FESOTERODINE FUMARATE
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 65862-767_33d91059-f2d5-482f-a47f-b1dccb7c5b22
- Product NDC
- 65862-767
- Form
- TABLET, FILM COATED, EXTENDED RELEASE
- Composition / generic term
- FESOTERODINE FUMARATE
- Labeler
- Aurobindo Pharma Limited
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220617
- Source listing expiry
- 20261231
Source-listed ingredients
- FESOTERODINE FUMARATE — 8 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-767-30) · 65862-767-30
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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