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: 71205-667_88f08450-559e-4038-aad1-051e4ab283cf
Product NDC: 71205-667
Form: TABLET, EXTENDED RELEASE
Composition / generic term: oxybutynin chloride
Labeler: Proficient Rx LP
Marketing category: ANDA
Marketing start / end (source format): 20161220
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 (71205-667-30) · 71205-667-30
60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-667-60) · 71205-667-60
90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-667-90) · 71205-667-90

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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