United States · FDA National Drug Code directory
Tolterodine Tartrate
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
- 16571-127_d56e7ced-4633-4325-8e3d-166c84c05886
- Product NDC
- 16571-127
- Form
- TABLET, FILM COATED
- Composition / generic term
- Tolterodine Tartrate
- Labeler
- Rising Pharma Holdings, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200124
- Source listing expiry
- 20261231
Source-listed ingredients
- TOLTERODINE TARTRATE — 2 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (16571-127-01) · 16571-127-01
- 60 TABLET, FILM COATED in 1 BOTTLE (16571-127-06) · 16571-127-06
- 500 TABLET, FILM COATED in 1 BOTTLE (16571-127-50) · 16571-127-50
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →