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
31722-607_e16012ae-5972-470b-8a22-b0626a029e95
Product NDC
31722-607
Form
CAPSULE, EXTENDED RELEASE
Composition / generic term
Tolterodine Tartrate
Labeler
Camber Pharmaceuticals, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20170602
Source listing expiry
20261231

Source-listed ingredients

  • TOLTERODINE TARTRATE — 2 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (31722-607-05) · 31722-607-05
  • 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (31722-607-30) · 31722-607-30
  • 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (31722-607-90) · 31722-607-90

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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