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
54838-510_693f3eb4-b7f1-420a-b813-ecd8e326882d
Product NDC
54838-510
Form
SYRUP
Composition / generic term
Oxybutynin Chloride
Labeler
Lannett Company, Inc.
Marketing category
ANDA
Marketing start / end (source format)
19960329
Source listing expiry
20261231

Source-listed ingredients

  • OXYBUTYNIN CHLORIDE — 5 mg/5mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 473 mL in 1 BOTTLE, PLASTIC (54838-510-80) · 54838-510-80

Source and coverage

Open FDA National Drug Code directory

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.

Browse United States records →