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
43063-790_419e3f00-a475-03d5-e063-6394a90a5f89
Product NDC
43063-790
Form
TABLET, EXTENDED RELEASE
Composition / generic term
Oxybutynin Chloride
Labeler
PD-Rx Pharmaceuticals, Inc.
Marketing category
ANDA
Marketing start / end (source format)
20090301
Source listing expiry
20261231

Source-listed ingredients

  • OXYBUTYNIN CHLORIDE — 10 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (43063-790-90) · 43063-790-90

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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