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
- 71610-277_b28dba2b-b19b-469e-98d8-54e87e3800e3
- Product NDC
- 71610-277
- Form
- TABLET
- Composition / generic term
- Oxybutynin Chloride
- Labeler
- Aphena Pharma Solutions - Tennessee, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20171023
- Source listing expiry
- 20261231
Source-listed ingredients
- OXYBUTYNIN CHLORIDE — 5 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET in 1 BOTTLE (71610-277-30) · 71610-277-30
- 60 TABLET in 1 BOTTLE (71610-277-53) · 71610-277-53
- 90 TABLET in 1 BOTTLE (71610-277-60) · 71610-277-60
- 180 TABLET in 1 BOTTLE (71610-277-80) · 71610-277-80
- 270 TABLET in 1 BOTTLE (71610-277-92) · 71610-277-92
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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