United States · FDA National Drug Code directory

Oxybutynin Chloride Extended Release

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
43353-284_a9056bad-e15c-4be4-a63c-f51362e2f025
Product NDC
43353-284
Form
TABLET, EXTENDED RELEASE
Composition / generic term
Oxybutynin Chloride
Labeler
Aphena Pharma Solutions - Tennessee, LLC
Marketing category
ANDA
Marketing start / end (source format)
20160309
Source listing expiry
20261231

Source-listed ingredients

  • OXYBUTYNIN CHLORIDE — 10 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (43353-284-30) · 43353-284-30
  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (43353-284-60) · 43353-284-60

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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