United States · FDA National Drug Code directory
Oxybutynin 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
- 0832-0038_45af3420-b44f-39a1-e063-6394a90ad626
- Product NDC
- 0832-0038
- Form
- TABLET
- Composition / generic term
- Oxybutynin Chloride
- Labeler
- Upsher-Smith Laboratories, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20111107 / 20281231
Source-listed ingredients
- OXYBUTYNIN CHLORIDE — 5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (0832-0038-00) · 0832-0038-00
- 1000 TABLET in 1 BOTTLE (0832-0038-10) · 0832-0038-10
- 500 TABLET in 1 BOTTLE (0832-0038-50) · 0832-0038-50
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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