United States · FDA National Drug Code directory
Trospium Chloride
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
- 23155-530_7d64107c-fe1a-452d-83fa-c2d0424ecb57
- Product NDC
- 23155-530
- Form
- TABLET, FILM COATED
- Composition / generic term
- Trospium Chloride
- Labeler
- Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20160830
- Source listing expiry
- 20271231
Source-listed ingredients
- TROSPIUM CHLORIDE — 20 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 200 TABLET, FILM COATED in 1 BOTTLE (23155-530-02) · 23155-530-02
- 500 TABLET, FILM COATED in 1 BOTTLE (23155-530-05) · 23155-530-05
- 60 TABLET, FILM COATED in 1 BOTTLE (23155-530-06) · 23155-530-06
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 →