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
0615-8492_126741bf-877c-4f91-a0e0-a2378747e33b
Product NDC
0615-8492
Form
TABLET
Composition / generic term
OXYBUTYNIN CHLORIDE
Labeler
NCS HealthCare of KY, LLC dba Vangard Labs
Marketing category
ANDA
Marketing start / end (source format)
20191101
Source listing expiry
20261231

Source-listed ingredients

  • OXYBUTYNIN CHLORIDE — 5 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

  • 15 TABLET in 1 BLISTER PACK (0615-8492-05) · 0615-8492-05
  • 30 TABLET in 1 BLISTER PACK (0615-8492-39) · 0615-8492-39

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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