United States · FDA National Drug Code directory
solifenacin succinate
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
- 31722-028_e52cdf06-9178-ab2f-e053-2a95a90af2b3
- Product NDC
- 31722-028
- Form
- TABLET, FILM COATED
- Composition / generic term
- solifenacin succinate
- Labeler
- Camber Pharmaceuticals, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20220615
- Source listing expiry
- 20261231
Source-listed ingredients
- SOLIFENACIN SUCCINATE — 10 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED in 1 BOTTLE (31722-028-30) · 31722-028-30
- 10 BLISTER PACK in 1 CARTON (31722-028-31) / 10 TABLET, FILM COATED in 1 BLISTER PACK (31722-028-32) · 31722-028-31
- 90 TABLET, FILM COATED in 1 BOTTLE (31722-028-90) · 31722-028-90
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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