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: 33342-097_fa641ff6-005b-47c5-bade-8709129d7ac9
Product NDC: 33342-097
Form: TABLET, FILM COATED
Composition / generic term: Tolterodine tartrate
Labeler: Macleods Pharmaceuticals Limited
Marketing category: ANDA
Marketing start / end (source format): 20201008
Source listing expiry: 20261231

Source-listed ingredients

TOLTERODINE TARTRATE — 1 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

60 TABLET, FILM COATED in 1 BOTTLE (33342-097-09) · 33342-097-09
10 BLISTER PACK in 1 CARTON (33342-097-12) / 10 TABLET, FILM COATED in 1 BLISTER PACK · 33342-097-12
500 TABLET, FILM COATED in 1 BOTTLE (33342-097-15) · 33342-097-15

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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